Heterocyclic compounds and methods of their use

ABSTRACT

The present invention relates to heterocyclic compounds useful for antagonising angiotensin II Type 2 (AT 2 ) receptor. More particularly the invention relates to pyrrolidine and azetidine compounds, compositions containing them and their use in methods of treating or preventing disorders or diseases associated with AT 2  receptor function including neuropathic pain, inflammatory pain, conditions associated with neuronal hypersensitivity, impaired nerve conduction velocity, cell proliferation disorders, disorders associated with an imbalance between bone resorption and bone formation and disorders associated with aberrant nerve regeneration.

FIELDS OF THE INVENTION

The present invention relates generally to compounds that are useful inantagonizing the angiotensin II type 2 (AT₂) receptor. Moreparticularly, the invention relates to heterocyclic compounds of formula(I) and their use as AT₂ receptor antagonists. Pharmaceuticalcompositions comprising the compounds and their use in modulating theAT₂ receptor and therapies that require modulation of the AT₂ receptorare described.

BACKGROUND OF THE INVENTION

Although AT₂ receptor has been known since the 1980s, much less is knownabout its biological function than the angiotensin. II type 1 (AT₁)receptor, which has been studied for its functional effects onvasoconstriction, aldosterone release and cardiovascular growth [Wexleret al., 1996]. However, more recently the AT₂ receptor has beenimplicated in the differentiation and regeneration of neuronal tissue[Steckelings et al., 2005; Chakrabarty et al., 2008], cell proliferationand angiogenesis [Clere et al., 2010] and maintenance of bone mass [Izuet al., 2009].

AT₂ receptor antagonists have also recently been associated with thetreatment of pain, particularly inflammatory pain [WO 2007/106938] andneuropathic pain [WO 2006/066361], two types of pain which are difficultto treat or relieve. Impaired nerve conduction velocity is alsoassociated with nerve damage and has been implicated in peripheralneuropathies, Carpel Tunnel Syndrome, ulnar neuropathy, Guillian-BarréSyndrome, fascioscapulohumeral muscular dystrophy and spinal discherneation. Impaired nerve conduction velocity can result in diminishedreflex responses and altered peripheral sensation such as parathesia andin some cases pain and AT₂ receptor antagonists have been shown torestore nerve conduction velocity [WO 2011/088504].

While there are effective therapies for treating nociceptive pain,inflammatory and neuropathic pain are often resistant to thesetherapies. In addition, current therapies of neuropathic pain,inflammatory pain, impaired nerve conduction velocity and other types ofpain that are difficult to treat, have serious side effects, forexample, cognitive changes, sedation, nausea and in the case of narcoticdrugs, tolerance and dependence. There is a need for further therapiesthat treat or prevent neuropathic pain, inflammatory pain, impairednerve conduction velocity and other painful conditions that arecurrently difficult to treat.

Cell proliferation and angiogenesis are important biological functionsin normal tissue. However, uncontrolled cell proliferation andangiogenesis can lead to tumors and other proliferative disorders. Whilethere are some effective chemotherapies available for tumors, manyresult in unpleasant side effects and/or have high toxicity for normalcells.

Further therapies for reducing or preventing abnormal cell proliferationin a controlled manner are required and AT₂ receptor antagonists havebeen shown to have antiproliferative activity [Clere et al., 2010].

Osteoporosis is a significant problem in older populations, especiallyin post-menopausal women. Current therapies for osteoporosis rely oncalcium supplementation. However, the control of bone formation and boneresorption is complex and further therapies for improving bone mass arerequired and AT₂ receptor antagonists have been shown to increase bonemass [Izu et al., 2009].

The role of the AT₂ receptor in modulating neuronal outgrowth andassociated effects of AT₂ receptor antagonists on reducing neuronaloutgrowth, indicates that AT₂ receptor antagonists may be usefultherapeutics in diseases characterized by aberrant nerve regeneration[Chakrabarty et al., 2008].

The present invention is predicated in part on the discovery ofheterocyclic azetidine and pyrrolidine compounds that have AT₂ receptorantagonist activity.

SUMMARY OF THE INVENTION

In a first aspect of the present invention there is provided a compoundof formula (I):

wherein:

X is absent and Y is —CHR³CH₂—, —CH₂CHR³—, —CHR³CHR⁴CH₂—, —CH₂CHR³CHR⁴—,—CH₂CH₂CHR³—, —CR³═CHCH₂—, —CH═CHR³CH₂— or —CH₂CH═CR³—; or

X is —CHR⁵ and Y is —CHR³—, —CHR³CHR⁴—, —CH₂CHR³—, —CHR³CR⁴—; —CR³—CH—or —CH═CR³—; wherein when Y is —CHR³CR⁴═, R^(2b) is absent; or

X is —CH₂CHR⁵— or C(═O)CHR⁵— and Y is —CHR³—;

R¹ is —C(═O)CHR⁶R⁷, —C(═O)NR⁶R⁷, —C(═O)CH₂CHR⁶R⁷, —C(═O)CH═CR⁶R⁷,—C(═S)CHR⁶R⁷, —C(═S)NR⁶R⁷, —C(═S)CH₂CHR⁶R⁷, —C(═S)CH═CR⁶R⁷,—C(═NR⁸)CHR⁶R⁷, —C(═NR⁸)NR⁶R⁷, —C(═NR⁸)CH₂CHR⁶R⁷ and —C(═NR⁸)CH═CR⁶R⁷;

R² is —C₁₋₆alkyl, —C₂₋₆alkenyl, —C₂₋₆alkynyl, —OR⁸, —SR⁸, —N(R⁸)₂,—C(═O)R⁸, —C(═O)N(R⁸)₂, —N(R⁸)C(═O)R⁸, —N(R⁸)C(═O)N(R⁸)₂, —N(R⁸)SO₂R⁸,—SO₂N(R⁸)₂, —N(R⁸)SO₂N(R⁸)₂, —W— cycloalkyl, —W-cycloalkenyl, —W-aryl,—W-heterocyclyl, —W-heteroaryl, —W—Z—W-cycloalkyl, —W—Z—W-cycloalkenyl,—W—Z—W-aryl, —W—Z—W-heterocyclyl or —W—Z—W-heteroaryl, ═CH—C(═O)-J-R¹⁰,═CHC(═O)NH-J-R¹⁰, —OCH₂CHR¹⁰CH₂R¹⁰ or —OCH₂C(R¹⁰)═CHR¹⁰;

R^(2b) is hydrogen;

R³ is a carboxylic acid, —CH₂CO₂H, —C(═O)C(═O)OH, —CH₂OH, —C(O)NH₂, —CN,—CH₂C(O)NH₂, —CH₂CN, a -carboxylic acid bioisostere or —CH₂carboxylicacid bioisostere;

R⁴ is hydrogen or R³ and R⁴ together form a group:

where R¹¹ is a carboxylic acid, —CH₂CO₂H, —C(═O)C(═O)OH, —CH₂OH,—C(O)NH₂, —CN, —CH₂C(O)NH₂, —CH₂CN, a carboxylic acid bioisostere or—CH₂carboxylic acid bioisostere;

R⁵ is hydrogen or together with R² forms a fused aryl, heterocyclyl orheteroaryl ring, optionally substituted with one or two optionalsubstituents selected from —C₁₋₆alkyl, —C₂₋₆alkenyl, —C₂₋₆alkynyl,cycloalkyl, cycloalkenyl, aryl, heterocyclyl, heteroaryl,—C₁₋₆alkyleneR¹⁰, —C₂₋₆alkenyleneR¹⁰, —C₂₋₆allcynyleneR¹⁰, —OCHF₂, —OR⁹,—OC₁₋₆alkyleneR¹⁰, —OC₂₋₆alkenyleneR¹⁰, —OC₂₋₆alkynyleneR¹⁰, —SO₂NHR⁹,—NHSO₂R⁹, —NHC(═O)NHR⁹, —NHC(═O)OR⁹ or —CH(OH)CH(OH)R⁹;

R⁶ and R⁷ are independently hydrogen, —C₁₋₆alkyl, cycloalkyl,cycloalkenyl, aryl, heterocyclyl, heteroaryl, —CH₂aryl, —CH₂cycloalkyl,—CH₂cycloalkenyl, —CH₂heterocyclyl or —CH₂heteroaryl; provided that R⁶and R⁷ are not both hydrogen;

R⁸ is hydrogen, —C₁₋₈alkyl, —C₁₋₈fluoroalkyl, aryl, C₁₋₈alkylenearyl,—C₂₋₈alkenylenearyl or —C₂₋₈alkynylenearyl;

R⁹ is —C₁₋₆alkyl, —C₂₋₆alkenyl, —C₂₋₆alkynyl, cycloalkyl, cycloalkenyl,aryl, heterocyclyl, heteroaryl, arylcycloalkyl-, arylcycloalkenyl-,arylaryl-, arylheterocyclyl- or arylheteroaryl-;

W is a covalent bond, —O—, —S—, —SO—, —SO₂—N(R⁸)—, —C(═O)—,—N(R⁸)C(═O)—, —C(═O)N(R⁸)—, —C₂₋₄alkenylene-, —C₂₋₄alkynylene-,—C₁₋₃alkyleneQC₁₋₃alkylene-, -QC₁₋₄alkylene-, -QC₂₋₄alkenylene-,-QC₂₋₄alkynylene-, —C₂₋₄alkenyleneQ-, —C₂₋₄alkynyleneQ-QC₁₋₄alkyleneQ-,-QC₂₋₄alkenyleneQ- or —OC₂₋₄alkynyleneQ-;

Q is —O—, —S—, —SO—, —SO₂—N(R⁸)—, —C(═O)—, —N(R⁸)C(═O)—, —C(═O)N(R⁸)—,

Z is cycloalkyl-, -cycloalkenyl-, -aryl-, -heterocyclyl- or-heteroaryl-;

J is a covalent bond or —C₁₋₆alkylene-, —C₂₋₆alkenylene- or—C₂₋₆alkynylene, in which one —CH₂— group in the alkylene, alkenylene oralkynylene group may be replaced by —O—, —S—, —S(O)—, —S(O)₂—N(R⁸)—,—C(═O)NH— or —NHC(═O)—;

R¹⁰ is cycloalkyl, cycloalkenyl, aryl, heterocyclyl or heteroaryl; and

wherein each cycloalkyl, cycloalkenyl, aryl, heterocyclyl and heteroarylmay be optionally substituted;

or a pharmaceutically acceptable salt thereof.

In another aspect, the present invention provides a pharmaceuticalcomposition comprising the compounds of formula (I) or apharmaceutically acceptable salt thereof and a pharmaceuticallyacceptable carrier.

In a further aspect of the invention, there is provided a method oftreating or preventing neuropathic pain in a subject comprisingadministering a compound of formula (I) or a pharmaceutically acceptablesalt thereof.

In yet a further aspect of the invention there is provided a method oftreating or preventing a condition characterized by neuronalhypersensitivity in a subject comprising administering a compound offormula (I) or a pharmaceutically acceptable salt thereof.

In yet another aspect of the invention, there is provided a method oftreating or preventing inflammatory pain in a subject comprisingadministering a compound of formula (I) or a pharmaceutically acceptablesalt thereof.

In a further aspect, the present invention provides a method of treatingor preventing impaired nerve conduction velocity in a subject comprisingadministering a compound of formula (I) or a pharmaceutically acceptablesalt thereof.

In yet a further aspect of the invention there is provided a method ofproducing analgesia in a subject comprising administering a compound offormula (I) or a pharmaceutically acceptable salt thereof.

In still another aspect of the invention there is provided a method oftreating or preventing a cell proliferative disorder in a subjectcomprising administering a compound of formula (I) or a pharmaceuticallyacceptable salt thereof.

In a further aspect the present invention provides a method of treatingor preventing a disorder associated with an imbalance between boneresorption and bone formation in a subject comprising administering acompound of formula (I) or a pharmaceutically acceptable salt thereof.

In yet another aspect the present invention provides a method oftreating a disorder associated with aberrant nerve regeneration in asubject comprising administering a compound of formula (I) or apharmaceutically acceptable salt thereof.

DESCRIPTION OF THE INVENTION Definitions

Unless defined otherwise, all technical and scientific terms used hereinhave the same meaning as commonly understood by those of ordinary skillin the art to which the invention belongs. Although any methods andmaterials similar or equivalent to those described herein can be used inthe practice or testing of the present invention, preferred methods andmaterials are described. For the purposes of the present invention, thefollowing terms are defined below.

The articles “a” and “an” are used herein to refer to one or to morethan one (i.e. to at least one) of the grammatical object of thearticle. By way of example, “an element” means one element or more thanone element.

As used herein, the term “about” refers to a quantity, level, value,dimension, size, or amount that varies by as much as 30%, 25%, 20%, 15%or 10% to a reference quantity, level, value, dimension, size, oramount.

As used herein, the term “AT₂ receptor” means an angiotensin II type 2(AT₂) receptor polypeptide that can bind angiotensin II and/or one ormore other ligands. The term “AT₂ receptor” encompasses vertebratehomologs of AT₂ receptor family members, including, but not limited to,mammalian, reptilian and avian homologs. Representative mammalianhomologs of AT₂ receptor family members include, but are not limited to,murine and human homologs.

The term “antagonist” as used herein refers to a compound that decreasesor inhibits the biological activity and/or function of an AT₂ receptor,including binding to the AT₂ receptor and blocking access to angiotensinII, inhibiting a gene that expresses AT₂ receptor, or inhibiting anexpression product of that gene. By the term “selective”, is meant thatthe compound binds to and/or inhibits AT₂ receptor activity to a greaterextent than binding and inhibition of the AT₁ receptor. In someinstances, selective refers to binding and/or inhibition of the AT₂receptor with little or no binding at the AT₁ receptor.

The term “allodynia” as used herein refers to the pain that results froma non-noxious stimulus i.e. pain due to a stimulus that does notnormally provoke pain. Examples of allodynia include, but are notlimited to, cold allodynia, tactile allodynia (pain due to lightpressure or touch), and the like.

The term “analgesia” is used herein to describe states of reduced painperception, including absence from pain sensations as well as states ofreduced or absent sensitivity to noxious stimuli. Such states of reducedor absent pain perception are induced by the administration of apain-controlling agent or agents and occur without loss ofconsciousness, as is commonly understood in the art. The term analgesiaencompasses the term “antinociception”, which is used in the art as aquantitative measure of analgesia or reduced pain sensitivity in animalmodels.

The term “anti-allodynia” is used herein to describe states of reducedpain perception, including absence from pain sensations as well asstates of reduced or absent sensitivity to non-noxious stimuli. Suchstates of reduced or absent pain perception are induced by theadministration of a pain-controlling agent or agents and occur withoutloss of consciousness, as is commonly understood in the art.

The term “causalgia” as used herein refers to the burning pain,allodynia, and hyperpathia after a traumatic nerve lesion, oftencombined with vasomotor and sudomotor dysfunction and later trophicchanges.

By “complex regional pain syndromes” is meant the pain that includes,but is not limited to, reflex sympathetic dystrophy, causalgia,sympathetically maintained pain, and the like.

By “condition characterized by neuronal hypersensitivity” is meantconditions that have symptoms of pain related to neuronalhypersensitivity and/or allodynia. Examples of this type of conditioninclude fibromyalgia and irritable bowel syndrome.

By “disorder associated with aberrant nerve regeneration” is meantdisorders in which there is abnormal axon outgrowth in neurons. Thisabnormal outgrowth may be associated with painful conditions includingbreast pain, interstitial cystitis, vulvodynia and cancerchemotherapy-induced neuropathies.

Throughout this specification, unless the context requires otherwise,the words “comprise”, “comprises” and “comprising” will be understood toimply the inclusion of a stated step or element or group of steps orelements but not the exclusion of any other step or element or group ofsteps or elements.

By “hyperalgesia” is meant an increased response to a stimulus that isnormally painful. A hyperalgesia condition is one that is associatedwith pain caused by a stimulus that is not normally painful.

By “neuropathic pain” is meant any pain syndrome initiated or caused bya primary lesion or dysfunction in the peripheral or central nervoussystem. Examples of neuropathic pain include, but are not limited to,thermal or mechanical hyperalgesia, thermal or mechanical allodynia,diabetic pain, entrapment pain, and the like.

The term “nociceptive pain” refers to the normal, acute pain sensationevoked by activation of nociceptors located in non-damaged skin, visceraand other organs in the absence of sensitization.

As used herein “inflammatory pain” refers to pain induced byinflammation. Such types of pain may be acute or chronic and can be dueto any number of conditions characterized by inflammation including,without limitation, burns including chemical, frictional or thermalburns, autoimmune diseases such as rheumatoid arthritis, osteoarthritisand inflammatory bowel disease including Crohn's disease and colitis, aswell as other inflammatory diseases including carditis, dermatitis,myositis, neuritis and collagen vascular diseases.

The term “pain” as used herein is given its broadest sense and includesan unpleasant sensory and emotional experience associated with actual orpotential tissue damage, or described in terms of such damage andincludes the more or less localized sensation of discomfort, distress,or agony, resulting from the stimulation of specialized nerve endings.There are many types of pain, including, but not limited to, lightningpains, phantom pains, shooting pains, acute pain, inflammatory pain,neuropathic pain, complex regional pain, neuralgia, neuropathy, and thelike (Dorland's Illustrated Medical Dictionary, 28^(th) Edition, W. B.Saunders Company, Philadelphia, Pa.). The goal of treatment of pain isto reduce the degree of severity of pain perceived by a treatmentsubject.

By the phrases “impaired NCV” or “impaired nerve conduction velocity”and the like is meant any nerve conduction demonstrably abnormal in anyone of the parameters assessed for normal nerve signal conduction.Whether the various parameters of NCV are normal is typically anassessment made by the relevant trained clinician. General background,terminology and procedures known to those in the art for evaluating NCVare described in “Proper performance and interpretation ofelectrodiagnostic studies' Muscle Nerve. (2006) 33(3):436-439 and“Electrodiagnostic medicine listing of sensory, motor, and mixednerves.” Appendix J of Current Procedural Terminology (CPT) 2007,authored by The American Association of Neuromuscular &Electrodiagnostic Medicine and published by the American MedicalAssociation. Impaired or abnormal nerve conduction velocity is a symptomof nerve dysfunction or damage and may be causal to or a symptom of alarge number of diseases or disorders, particularly diseases ordisorders that exhibit diminished reflex responses and alteredperipheral sensation including paresthesia. As used herein,“paresthesia” refers to a sensation of tingling, prickling, weakness ornumbness in a subject's skin. It is also known as “pins and needles” ora limb “falling asleep”. Paresthesia may be transient, acute or chronicand may occur alone or be accompanied by other symptoms such as pain.

As used herein, the term “cell proliferative disorder” refers todiseases or conditions where unwanted or damaged cells are not removedby normal cellular process, or diseases or conditions in which cellsundergo aberrant, unwanted or inappropriate proliferation. Disorderscharacterized by inappropriate cell proliferation include, for example,inflammatory conditions such as inflammation arising from acute tissueinjury including, for example, acute lung injury, cancer includingcancers characterized by tumors, autoimmune disorders, tissuehypertrophy and the like.

The term “disorder associated with an imbalance between bone resorptionand bone formation” includes disorders where there is insufficientdevelopment of bone mass, excessive bone resorption and insufficientbone formation during remodelling. An exemplary disorder associated withan imbalance between bone resorption and bone formation is osteoporosis.

As used herein, the term “alkyl” refers to a straight chain or branchedsaturated hydrocarbon group having 1 to 10 carbon atoms. Whereappropriate, the alkyl group may have a specified number of carbonatoms, for example, C₁₋₆alkyl which includes alkyl groups having 1, 2,3, 4, 5 or 6 carbon atoms in a linear or branched arrangement. Examplesof suitable alkyl groups include, but are not limited to, methyl, ethyl,n-propyl, i-propyl, n-butyl, i-butyl, t-butyl, n-pentyl, 2-methylbutyl,3-methylbutyl, 4-methylbutyl, n-hexyl, 2-methylpentyl, 3-methylpentyl,4-methylpentyl, 5-methylpentyl, 2-ethylbutyl, 3-ethylbutyl, heptyl,octyl, nonyl and decyl.

The term “fluoroalkyl” as used herein refers to an alkyl group in whichone or more hydrogen atoms of the alkyl group is replaced with a fluoroatom. Where appropriate, the alkyl group may have a specified number ofcarbon atoms, for example, C₁₋₆fluoroalkyl which includes fluoroalkylgroups having 1, 2, 3, 4, 5 or 6 carbon atoms in a linear or branchedarrangement. Examples of fluoroalkyl groups include fluoromethyl,difluoromethyl, trifluoromethyl, 1-fluoroethyl, 2-fluoroethyl,1,1-difluoroethyl, 2,2-fluoroethyl, 1,1,2-trifluoroethyl,2,2,2-trifluoroethyl, 1,1,2,2,2-pentafluoroethyl, 3-fluoropropyl,3,3-difluoropropyl, 3,3,3-trifluoropropyl, 4-fluorobutyl,4,4-difluorobutyl, 4,4,4-trifluorobutyl, 5-fluoropentyl,5,5-difluoropentyl, 5,5,5-trifluoropentyl, 6-fluorohexyl,6,6-difluorohexyl or 6,6,6-trifluorohexyl and the like.

As used herein, the term “alkenyl” refers to a straight-chain orbranched hydrocarbon group having one or more double bonds betweencarbon atoms and having 2 to 10 carbon atoms. Where appropriate, thealkenyl group may have a specified number of carbon atoms. For example,C₂-C₆ as in “C₂-C₆alkenyl” includes groups having 2, 3, 4, 5 or 6 carbonatoms in a linear or branched arrangement. Examples of suitable alkenylgroups include, but are not limited to, ethenyl, propenyl, isopropenyl,butenyl, butadienyl, pentenyl, pentadienyl, hexenyl, hexadienyl,heptenyl, octenyl, nonenyl and decenyl.

As used herein, the term “alkynyl” refers to a straight-chain orbranched hydrocarbon group having one or more triple bonds and having 2to 10 carbon atoms. Where appropriate, the alkynyl group may have aspecified number of carbon atoms. For example, C₂-C₆ as in“C₂-C₆alkynyl” includes groups having 2, 3, 4, 5 or 6 carbon atoms in alinear or branched arrangement. Examples of suitable alkynyl groupsinclude, but are not limited to ethynyl, propynyl, butynyl, pentynyl andhexynyl.

As used herein, the term “cycloalkyl” refers to a saturated cyclichydrocarbon. The cycloalkyl ring may include a specified number ofcarbon atoms. For example, a 3 to 8 membered cycloalkyl group includes3, 4, 5, 6, 7 or 8 carbon atoms. Examples of suitable cycloalkyl groupsinclude, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl,cyclohexyl, cycloheptyl and cyclooctyl.

As used herein, the term “cycloalkenyl” refers to an unsaturated cyclichydrocarbon. The cycloalkenyl ring may include a specified number ofcarbon atoms. For example, a 5 to 8 membered cycloalkenyl group includes5, 6, 7 or 8 carbon atoms. The cycloalkenyl group has one or more doublebonds and when more than one double bond is present, the double bondsmay be unconjugated or conjugated, however the cycloalkenyl group is notaromatic. Examples of suitable cycloalkenyl groups include, but are notlimited to, cyclopentenyl, cyclohexenyl, cyclohexadienyl, cycloheptenyl,cycloheptadienyl, cycloheptatrienyl, cyclooctenyl, cyclooctadienyl andcyclooctatrienyl rings.

As used herein, the term “aryl” is intended to mean any stable,monocyclic, bicyclic or tricyclic carbon ring system of up to 7 atoms ineach ring, wherein at least one ring is aromatic. Examples of such arylgroups include, but are not limited to, phenyl, naphthyl,tetrahydronaphthyl, indanyl, fluorenyl, phenanthrenyl, biphenyl andbinaphthyl.

As used herein, the term “alkylene” refers to a divalent saturatedhydrocarbon chain having 1 to 6 carbon atoms. Where appropriate, thealkylene group may have a specified number of carbon atoms, for example,C₁₋₆alkylene includes alkylene groups having 1, 2, 3, 4, 5 or 6 carbonatoms in a linear arrangement. Examples of suitable alkylene groupsinclude, but are not limited to, —CH₂—, —CH₂CH₂—, —CH₂CH₂CH₂—,—CH₂CH₂CH₂CH₂—, —CH₂CH₂CH₂CH₂CH₂— and —CH₂CH₂CH₂CH₂CH₂CH₂—.

As used herein, the term “alkenylene” refers to a divalent unsaturatedhydrocarbon chain having 2 to 6 carbon atoms and at least one doublebond. Where appropriate, the alkenylene group may have a specifiednumber of carbon atoms, for example, C₂₋₆alkenylene includes alkenylenegroups having 2, 3, 4, 5 or 6 carbon atoms in a linear arrangement. Thedouble bonds may be in either E or Z configuration. Examples of suitablealkenylene groups include, but are not limited to, —CH═CH—, —CH═CHCH₂—,—CH₂CH═CH—, —CH═CHCH₂CH₂—, —CH₂CH═CHCH₂—, —CH₂CH₂CH═CH—,—CH═CHCH₂CH₂CH₂—, —CH₂CH═CHCH₂CH₂—, —CH₂CH₂CH═CHCH₂—, —CH₂CH₂CH₂CH═CH—,—CH═CHCH₂CH₂CH₂CH₂— —CH₂CH═CHCH₂CH₂CH₂—, —CH₂CH₂CH═CHCH₂CH₂—,—CH₂CH₂CH₂CH═CHCH₂— and —CH₂CH₂CH₂CH₂CH═CH—.

As used herein, the term “alkynylene” refers to a divalent unsaturatedhydrocarbon chain having 2 to 6 carbon atoms and at least one triplebond. Where appropriate, the alkynylene group may have a specifiednumber of carbon atoms, for example, C₂₋₆alkynylene includes alkynylenegroups having 2, 3, 4, 5 or 6 carbon atoms in a linear arrangement.Examples of suitable alkynylene groups include, but are not limited to,—C≡C—, —C≡CCH₂—, —CH₂C≡C—, —C≡CCH₂CH₂—, —CH₂C≡CCH₂—, —CH₂CH₂C≡C—,—C≡CCH₂CH₂CH₂—, —CH₂C≡CCH₂CH₂—, —CH₂CH₂C≡CCH₂—, —CH₂CH₂CH₂C≡C—,—C≡CCH₂CH₂GH₂CH₂—, —CH₂C≡CCH₂CH₂CH₂—, —CH₂CH₂C≡CCH₂CH₂—,—CH₂CH₂CH₂C≡CCH₂— and —CH₂CH₂CH₂CH₂C≡C—.

In some embodiments, one or more “—CH₂—” groups in an alkylene,alkenylene or alkynylene group may be replaced by a heteroatom or agroup containing a heteroatom including —O—, —S—, —NH—, —NR—, —S(O)—,—S(O)₂—, —C(═O)—, —C(═O)NH— and —NHC(═O)—.

The term “benzyl” where used herein refers to a phenylmethylene group,C₆H₅CH₂—.

As used herein, the term “halogen” or “halo” refers to fluorine(fluoro), chlorine (chloro), bromine (bromo) and iodine (iodo).

The term “heterocyclic” or “heterocyclyl” as used herein, refers to acyclic hydrocarbon in which one to four carbon atoms have been replacedby heteroatoms independently selected from the group consisting of N,N(R), S, S(O), S(O)₂ and O. A heterocyclic ring may be saturated orunsaturated but not aromatic. A heterocyclic group may also be part of aspirocyclic group containing 1, 2 or 3 rings, two of which are in a“spiro” arrangement. Examples of suitable heterocyclyl groups includeazetidine, tetrahydrofuranyl, tetrahydrothiophenyl, pyrrolidinyl,2-oxopyrrolidinyl, pyrrolinyl, pyranyl, dioxolanyl, piperidinyl,2-oxopiperidinyl, pyrazolinyl, imidazolinyl, thiazolinyl, dithiolyl,oxathiolyl, dioxanyl, dioxinyl, dioxazolyl, oxathiozolyl, oxazolonyl,piperazinyl, morpholino, thiomorpholinyl, 3-oxomorpholinyl, dithianyl,trithianyl and oxazinyl.

The term “heteroaryl” as used herein, represents a stable monocyclic,bicyclic or tricyclic ring of up to 7 atoms in each ring, wherein atleast one ring is aromatic and at least one ring contains from 1 to 4heteroatoms selected from the group consisting of O, N and S. Heteroarylgroups within the scope of this definition include, but are not limitedto, acridinyl, carbazolyl, cinnolinyl, quinoxalinyl, quinazolinyl,pyrazolyl, indolyl, isoindolyl, 1H,3H-1-oxoisoindolyl, benzotriazolyl,furanyl, thienyl, thiophenyl, benzothienyl, benzofuranyl, benzodioxane,benzodioxin, quinolinyl, isoquinolinyl, oxazolyl, isoxazolyl,imidazolyl, pyrazinyl, pyridazinyl, pyridinyl, pyrimidinyl, pyrrolyl,tetrahydroquinolinyl, thiazolyl, isothiazolyl, 1,2,3-triazolyl,1,2,4-triazolyl, 1,2,4-oxadiazolyl, 1,2,4-thiadiazolyl, 1,3,5-triazinyl,1,2,4-triazinyl, 1,2,4,5-tetrazinyl and tetrazolyl. Particularheteroaryl groups have 5- or 6-membered rings, such as pyrazolyl,furanyl, thienyl, oxazolyl, indolyl, isoindolyl, 1H,3H-1-oxoisoindolyl,isoxazolyl, imidazolyl, pyrazinyl, pyridazinyl, pyridinyl, pyrimidinyl,pyrrolyl, thiazolyl, isothiazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl and1,2,4-oxadiazolyl and 1,2,4-thiadiazolyl.

Each alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl,heterocyclyl and heteroaryl whether an individual entity or as part of alarger entity may be optionally substituted with one or more optionalsubstituents selected from the group consisting of C₁₋₆alkyl,C₂₋₆alkenyl, C₃₋₆cycloalkyl, oxo (═O), —OH, —SH, C₂₋₆alkenylO—,C₃₋₆cycloalkylO—, C₁₋₆alkylS-, C₂₋₆alkenylS-, C₃₋₆cycloalkylS-, —CO₂H,—CO₂C₁₋₆alkyl, —NH₂, —NH(C₁₋₆alkyl), —N(C₁₋₆alkyl)₂, —NH(phenyl),—N(phenyl)₂, oxo, —CN, —NO₂, -halogen, —CF₃, —OCF₃, —SCF₃, —CHF₂,—OCHF₂, —SCHF₂, -phenyl, -heterocyclyl, -heteroaryl, —Oheteroaryl,—Oheterocyclyl, —Ophenyl, —C(O)phenyl, —C(O)C₁₋₆alkyl. Examples ofsuitable substituents include, but are not limited to, methyl, ethyl,propyl, isopropyl, butyl, sec-butyl, tert-butyl, vinyl, methoxy, ethoxy,propoxy, isopropoxy, butoxy, methylthio, ethylthio, propylthio,isopropylthio, butylthio, hydroxy, hydroxymethyl, hydroxyethyl,hydroxypropyl, hydroxybutyl, fluoro, chloro, bromo, iodo, cyano, nitro,—CO₂H, —CO₂CH₃, trifluoromethyl, trifluoromethoxy, trifluoromethylthio,difluoromethyl, difluoromethoxy, difluoromethylthio, morpholino, amino,methylamino, dimethylamino, phenyl, phenoxy, phenylcarbonyl, benzyl andacetyl.

The term “carboxylic acid bioisotere” refers to a group which isphysiochemically or topologically similar to carboxylic acid orcarboxylate group. Examples of suitable carboxylic acid or carboxylateisosteres include, but are not limited to, tetrazole, tetrazolate,—CONH-tetrazole, oxadiazole, phosphate (—PO₃H₂), —C(OH)(CF₃)₂, N-(arylor heteroaryl)-sulfonamides, acylsulfonamides and sulfonic acid (—SO₃H)[See Patani and LaVoie, 1996]. Examples of sulfonamide isostericequivalents of carboxy groups include —CONHSO₂R^(a), —CONHSO₂N(R^(a))₂,—SO₂NHCOR^(a), —SO₂NHCONHR^(a), —SO₂NFIR^(a) and —NHSO₂R^(a), whereR^(a) is selected from the group consisting of C₁₋₆alkyl, C₂₋₆alkenyl,C₃₋₈cycloalkyl, aryl, heterocyclyl, heteroaryl and —CF₃.

The compounds of the invention may be in the form of pharmaceuticallyacceptable salts. It will be appreciated however thatnon-pharmaceutically acceptable salts also fall within the scope of theinvention since these may be useful as intermediates in the preparationof pharmaceutically acceptable salts or may be useful during storage ortransport. Suitable pharmaceutically acceptable salts include, but arenot limited to, salts of pharmaceutically acceptable inorganic acidssuch as hydrochloric, sulphuric, phosphoric, nitric, carbonic, boric,sulfamic, and hydrobromic acids, or salts of pharmaceutically acceptableorganic acids such as acetic, propionic, butyric, tartaric, maleic,hydroxymaleic, fumaric, maleic, citric, lactic, mucic, gluconic,benzoic, succinic, oxalic, phenylacetic, methanesulphonic,toluenesulphonic, benezenesulphonic, salicylic sulphanilic, aspartic,glutamic, edetic, stearic, palmitic, oleic, lauric, pantothenic, tannic,ascorbic and valeric acids.

Base salts include, but are not limited to, those formed withpharmaceutically acceptable cations, such as sodium, potassium, lithium,calcium, magnesium, ammonium and alkylammonium.

Basic nitrogen-containing groups may be quaternized with such agents aslower alkyl halide, such as methyl, ethyl, propyl, and butyl chlorides,bromides and iodides; dialkyl sulfates like dimethyl and diethylsulfate; and others.

It will also be recognised that compounds of the invention may possessasymmetric centres and are therefore capable of existing in more thanone stereoisomeric form. The invention thus also relates to compounds insubstantially pure isomeric form at one or more asymmetric centres eg.,greater than about 90% ee, such as about 95% or 97% ee or greater than99% ee, as well as mixtures, including racemic mixtures, thereof. Suchisomers may be prepared by asymmetric synthesis, for example usingchiral intermediates, or by chiral resolution. The compounds of theinvention may exist as geometric isomers. The invention also relates tocompounds in substantially pure cis (Z) or trans (E) or mixturesthereof.

Compounds of the Invention

In a first aspect of the present invention there is provided a compoundof formula (I):

wherein:

X is absent and Y is —CHR³CH₂—, —CH₂CHR³—, —CHR³CHR⁴CH₂—, —CH₂CHR³CHR⁴—,—CH₂CH₂CHR³—, —CR³═CHCH₂—, —CH═CHR³CH₂— or —CH₂CH═CR³—; or

X is —CHR⁵ and Y is —CHR³—, —CHR³CHR⁴—, —CH₂CHR³—, —CHR³CR⁴═, —CR³═CH—or —CH═CR³—; wherein when Y is —CHR³CR⁴═, R^(2b) is absent; or

X is —CH₂CHR⁵— or C(═O)CHR⁵— and Y is —CHR³—;

R¹ is —C(═O)CHR⁶R⁷, —C(═O)NR⁶R⁷, —C(═O)CH₂CHR⁶R⁷, —C(═O)CH═CR⁶R⁷,—C(═S)CHR⁶R⁷, —C(═S)NR⁶R⁷, —C(═S)CH₂CHR⁶R⁷, —C(═S)CH═CR⁶R⁷,—C(═NR⁸)CHR⁶R⁷, —C(═NR⁸)NR⁶R⁷, —C(═NR⁸)CH₂CHR⁶R⁷ and —C(═NR⁸)CH═CR⁶R⁷;

R² is —C₁₋₆alkyl, —C₂₋₆alkenyl, —C₂₋₆alkynyl, —OR⁸, —SR⁸, —N(R⁸)₂,—C(═O)R⁸, —C(═O)N(R⁸)₂, —N(R⁸)C(═O)R⁸, —N(R⁸)C(═O)N(R⁸)₂, —N(R⁸)SO₂R⁸,—SO₂N(R⁸)₂, —N(R⁸)SO₂N(R⁸)₂, —W-cycloalkyl, —W-cycloalkqnyl, —W-aryl,—W-heterocyclyl, —W-heteroaryl, —W—Z—W-cycloalkyl, —W—Z—W-cycloalkenyl,—W—Z—W-aryl, —W—Z—W-heterocyclyl or —W—Z—W-heteroaryl, ═CH—C(═O)-J-R¹⁰,═CHC(═O)NH-J-R¹⁰, —OCH₂CHR¹⁰CH₂R¹⁰ or —OCH₂C(R¹⁰)═CHR¹⁰;

R^(2b) is hydrogen;

R³ is a carboxylic acid, —CH₂CO₂H, —C(═O)C(═O)OH, —CH₂OH, —C(O)NH₂, —CN,—CH₂C(O)NH₂, —CH₂CN, a -carboxylic acid bioisostere or —CH₂carboxylicacid bioisostere;

R⁴ is hydrogen or R³ and R⁴ together form a group:

where R¹¹ is a carboxylic acid, —CH₂CO₂H, —C(═O)C(═O)OH, —CH₂OH,—C(O)NH₂, —CN, —CH₂C(O)NH₂, —CH₂CN, a carboxylic acid bioisostere or—CH₂carboxylic acid bioisostere;

R⁵ is hydrogen or together with R² forms a fused aryl, heterocyclyl orheteroaryl ring, optionally substituted with one or two optionalsubstituents selected from —C₁₋₆alkyl, —C₂₋₆alkenyl, —C₂₋₆alkynyl,cycloalkyl, cycloalkenyl, aryl, heterocyclyl, heteroaryl,—C₁₋₆alkyleneR¹⁰, —C₂₋₆alkenyleneR¹⁰, —C₂₋₆alkynyleneR¹⁰, —OCF₃, —OCHF₂,—OR⁹, —OC₁₋₆alkyleneR¹⁰, —OC₂₋₆alkenyleneR¹⁰, —OC₂₋₆alkynyleneR¹⁰,—SO₂NHR⁹, —NHSO₂R⁹, —NHC(═O)NHR⁹, —NHC(═O)OR⁹ or —CH(OH)CH(OH)R⁹;

R⁶ and R⁷ are independently hydrogen, —C₁₋₆alkyl, cycloalkyl,cycloalkenyl, aryl, heterocyclyl, heteroaryl, —CH₂aryl, —CH₂cycloalkyl,—CH₂cycloalkenyl, —CH₂heterocyclyl or —CH₂heteroaryl; provided that R⁶and R⁷ are not both hydrogen;

R⁸ is hydrogen, —C₁₋₈alkyl, C₁₋₈fluoroalkyl, aryl, —C₁₋₈alkylenearyl,—C₂₋₈alkenylenearyl or —C₂₋₄alkynylenearyl;

R⁹ is —C₁₋₆alkyl, —C₂₋₆alkenyl, —C₂₋₆alkynyl, cycloalkyl, cycloalkenyl,aryl, heterocyclyl, heteroaryl, arylcycloalkyl-, arylcycloalkenyl-,arylaryl-, arylheterocyclyl- or arylheteroaryl-;

W is a covalent bond, —O—, —S—, —SO—, —SO₂—N(R⁸)—, —C(═O)—,—N(R⁸)C(═O)—, —C(═O)N(R⁸)—, —C₁₋₄alkylene-, —C₂₋₄alkenylene-,—C₂₋₄alkynylene-, —C₁₋₃alkyleneQC₁₋₃alkylene-, -QC₁₋₄alkylene-,-QC₂₋₄alkenylene-, -QC₂₋₄alkynylene-, —C₁₋₄alkyleneQ-,—C₂₋₄alkenyleneQ-, —C₂₋₄alkynyleneQ-QC₁₋₄alkyleneQ-, -QC₂₋₄alkenyleneQ-or —OC₂₋₄alkynyleneQ-;

Q is —O—, —S—, —SO—, —SO₂—N(R⁸)—, —C(═O)—, —N(R⁸)C(═O)—, —C(═O)N(R⁸)—,

Z is -cycloalkyl-, -cycloalkenyl-, -aryl-, -heterocyclyl- or-heteroaryl-;

J is a covalent bond or —C₁₋₆alkylene-, —C₂₋₆alkenylene- or—C₂₋₆alkynylene, in which one —CH₂— group in the alkylene, alkenylene oralkynylene group may be replaced by —O—, —S—, —S(O)—, —S(O)₂—N(R⁸)—,—C(═O)—, —C(═O)NH— or —NHC(═O)—;

R¹⁰ is cycloalkyl, cycloalkenyl, aryl, heterocyclyl or heteroaryl; and

wherein each cycloalkyl, cycloalkenyl, aryl, heterocyclyl and heteroarylmay be optionally substituted;

or a pharmaceutically acceptable salt thereof.

In a particular embodiment, the compound of formula (I) is a compound offormula (Ia):

wherein:

X is absent and Y is —CHR³CH₂—, —CH₂CHR³—, —CHR³CHR⁴CH₂—, —CH₂CHR³CHR⁴—,—CH₂CH₂CHR³—, —CR³═CHCH₂—, —CH═CHR³CH₂— or —CH₂CH═CR³—; or

X is —CHR⁵ and Y is —CHR³—, —CHR³CHR⁴—, —CH₂CHR³—, —CR³═CH— or —CH═CR³—;or

X is —CH₂CHR⁵— or C(═O)CHR⁵— and Y is —CHR³—;

R¹ is —C(═O)CHR⁶R⁷, —C(═O)NR⁶R⁷, —CHCH₂CHR⁶R⁷, —C(═O)CH═CR⁶R⁷,—C(═S)CHR⁶R⁷, —C(═S)NR⁶R⁷, —C(═S)CH₂CR⁶R⁷, —C(═S)CH═CR⁶R⁷,—C(═NR⁸)CHR⁶R⁷, —C(═NR⁸)NR⁶R⁷, —C(═NR⁸)CH₂CHR⁶R⁷ or —C(═NR⁸)CH—CR⁶R⁷;

R² is —C₁₋₆alkyl, —C₂₋₆alkenyl, —C₂₋₆alkynyl, —OR⁸, —SR⁸, —N(R⁸)₂,—C(═O)R⁸, —C(═O)N(R⁸)₂, —N(R⁸)C(═O)R⁸, —N(R⁸)C(═O)N(R⁸)₂, —N(R⁸)SO₂R⁸,—SO₂N(R⁸)₂, —N(R⁸)SO₂N(R⁸)₂, —W-cycloalkyl, —W-cycloalkenyl, —W-aryl,—W-heterocyclyl, —W-heteroaryl, —W—Z—W-cycloalkyl, —W—Z—W-cycloalkenyl,—W—Z—W-aryl, —W—Z—W-heterocyclyl or *W—Z—W-heteroaryl, ═CH—C(═O)-J-R¹⁰,═CHC(═O)NH-J-R¹⁰, —OCH₂CHR¹⁰CH₂R¹⁰ or —OCH₂C(R¹⁰)═CHR¹⁰;

R³ is a carboxylic acid, —CH₂CO₂H, —C(═O)C(═O)OH or a carboxylic acidbioisostere;

R⁴ is hydrogen or R³ and R⁴ together form a group:

where R¹¹ is a carboxylic acid, —CH₂CO₂H, —C(═O)C(═O)OH, or carboxylicacid bioisostere;

R⁵ is hydrogen or together with R² forms a fused aryl, heterocyclyl orheteroaryl ring, optionally substituted with one or two optionalsubstituents selected from —C₁₋₆alkyl, —C₂₋₆alkenyl, —C₂₋₆alkynyl,cycloalkyl, cycloalkenyl, aryl, heterocyclyl, heteroaryl,—C₁₋₆alkyleneR¹⁰, —C₂₋₆alkenyleneR¹⁰, —C₂₋₆alkynyleneR¹⁰, —OCF₃, —OCHF₂,—OR⁹, —OC₁₋₆alkyleneR¹⁰, —OC₂₋₆alkenyleneR¹⁰, —OC₂₋₆alkynyleneR¹⁰,—SO₂NHR⁹, —NHSO₂R⁹, —NHC(═O)NHR⁹, —NHC(═O)OR⁹ or —CH(OH)CH(OH)R⁹;

R⁶ and R⁷ are independently hydrogen, —C₁₋₆alkyl, cycloalkyl,cycloalkenyl, aryl, heterocyclyl, heteroaryl, —CH₂aryl, —CH₂cycloalkyl,—CH₂cycloalkenyl, —CH₂heterocyclyl or —CH₂heteroaryl; provided that R⁶and R⁷ are not both hydrogen;

R⁸ is hydrogen, —C₁₋₆alkyl, aryl or —C₁₋₆alkylenearyl;

R⁹ is —C₁₋₆alkyl, —C₂₋₆alkenyl, —C₂₋₆alkynyl, cycloalkyl, cycloalkenyl,aryl, heterocyclyl, heteroaryl, arylcycloalkyl-, arylcycloalkenyl-,arylaryl-, arylheterocyclyl- or arylheteroaryl-;

W is a covalent bond, —O—, —S—, —SO—, —SO₂—N(R⁸)—, —C(═O)—,—N(R⁸)C(═O)—, —C(═O)N(R⁸)—, —C₁₋₄alkylene-, —C₂₋₄alkenylene-,—C₂₋₄alkynylene-, —C₁₋₃alkyleneQC₁₋₃alkylene-, -QC₁₋₄alkylene-,-QC₂₋₄alkenylene-, -QC₂₋₄alkynylene-, —C₁₋₄alkyleneQ-,—C₂₋₄alkenyleneQ-, —C₂₋₄alkynyleneQ-QC₁₋₄alkyleneQ-, -QC₂₋₄alkenyleneQ-or —OC₂₋₄alkynyleneQ-;

Q is —O—, —S—, —SO—, —SO₂—N(R⁸)—, —C(═O)—, —N(R⁸)C(═O)—, —C(═O)N(R⁸)—,

Z is -cycloalkyl-, -cycloalkenyl-, -aryl-, -heterocyclyl- or-heteroaryl-;

J is a covalent bond or —C₁₋₆alkylene-, —C₂₋₆alkenylene- or—C₂₋₆alkynylene, in which one —CH₂— group in the alkylene, alkenylene oralkynylene group may be replaced by —O—, —S—, —S(O)—, —S(O)₂—N(R⁸)—,—C(═O)—, —C(═O)NH— or —NHC(═O)—;

R¹⁰ is cycloalkyl, cycloalkenyl, aryl, heterocyclyl or heteroaryl; and

wherein each cycloalkyl, cycloalkenyl, aryl, heterocyclyl and heteroarylmay be optionally substituted;

or a pharmaceutically acceptable salt thereof.

In particular embodiments of formula (I) or formula (Ia), one or more ofthe following applies:

X is absent and Y is —CHR³CH₂—;

X is —CH₂— or —CHR⁵— and Y is —CHR³—, —CHR³CH₂—, —CHR³CR⁴═, —CH₂CHR³—,—CH═CR³— or —CR³═CH—, wherein when Y is —CHR³CR⁴═, R^(2b) is absent,

or

X is —CH₂CH₂—, —CH₂CHR⁵— or —C(═O)CHR⁵— and Y is —CHR³—;

R¹ is —C(═O)CHR⁶R⁷, —C(═O)NR⁶R⁷, especially —C(═O)CH(aryl)(aryl),—C(═O)CH(aryl)(cycloalkyl), —C(═O)CH(cycloalkyl)(cycloalkyl),—C(═O)CH(aryl)(alkyl), —C(═O)N(aryl)(aryl), —C(═O)N(aryl)(cycloalkyl),—C(═O)N(cycloalkyl)(cycloalkyl) or —C(═O)N(aryl)(alkyl), where each arylor cycloalkyl group is optionally substituted; more especially—C(═O)CH(phenyl)(phenyl), —C(═O)CH(phenyl)(cyclohexyl),—C(═O)N(phenyl)(phenyl) or —C(═O)N(phenyl)(cyclohexyl), wherein eachphenyl or cyclohexyl group is optionally substituted with one or moresubstituents selected from —C₁₋₃alkyl, —OC₁₋₃alkyl and halo, especiallymethyl, methoxy and fluoro; most especially where R¹ is—C(═O)CH(phenyl)(phenyl) and —C(═O)N(phenyl)(phenyl);

R² is cycloalkyl, cycloalkenyl, aryl, heterocyclyl, heteroaryl,heterocyclylaryl, -heterocyclylC₁₋₃alkylenearyl,—C₁₋₄alkylenecycloalkyl, —C₁₋₄alkylenecycloalkenyl, —C₁₋₄alkylenearyl,—C₁₋₄alkyleneheterocyclyl, —C₁₋₄alkyleneheteroaryl,—C₂₋₄alkenylenecycloalkyl, —C₂₋₄alkenylenecycloalkenyl,—C₂₋₄alkenylenearyl, —C₂₋₄alkenyleneheterocyclyl,—C₂₋₄alkenyleneheteroaryl, —C₂₋₄alkynylenecycloalkyl,—C₂₋₄alkynylenecycloalkenyl, —C₂₋₄alkynylenearyl,—C₂₋₄alkynyleneheterocyclyl, —C₂₋₄alkynyleneheteroaryl,═CHC(═O)NHCH₂cycloalkyl, ═CHC(═O)NHCH₂cycloalkenyl, ═CHC(═O)NHCH₂aryl,═CHC(═O)NHCH₂heterocyclyl, ═CHC(═O)NHCH₂heteroaryl, —Ocycloalkyl,—Ocycloalkenyl, —Oaryl, —Oheterocyclyl, —Oheteroaryl,—OC₁₋₃alkylenecycloalkyl, —OC₁₋₃alkylenecycloalkenyl,—OC₁₋₃alkylenearyl, —OC₁₋₃alkyleneheterocyclyl,—OC₁₋₃alkyleneheteroaryl, —OC₂₋₃alkenylenecycloalkyl,—OC₂₋₃alkenylenecycloalkenyl, —OC₂₋₃alkenylenearyl,—OC₂₋₃alkenyleneheterocyclyl, —OC₂₋₃alkenyleneheteroaryl,—OC₂₋₃alkynylenecycloalkyl, —OC₂₋₃alkynylenecycloalkenyl,—OC₂₋₃alkynylenearyl, —OC₂₋₃alkynyleneheterocyclyl,—OC₂₋₃alkynyleneheteroaryl, —OC₁₋₃alkylenecycloalkyl aryl, —OarylOaryl,—OarylOC₁₋₃alkylenearyl, —Scycloalkyl, —Scycloalkenyl, —Saryl,—Sheterocyclyl, —Sheteroaryl, —SC₁₋₃alkylenecycloalkyl,—SC₁₋₃alkylenecycloalkenyl, —SC₁₋₃alkylenearyl,—SC₁₋₃alkyleneheterocyclyl, —SC₁₋₃alkyleneheteroaryl,—SC₂₋₃alkenylenecycloalkyl, —SC₂₋₃alkenylenecycloalkenyl,—SC₂₋₃alkenylenearyl, —SC₂₋₃alkenyleneheterocyclyl,—SC₂₋₃alkenyleneheteroaryl, —SC₂₋₃alkynylenecycloalkyl,—SC₂₋₃alkynylenecycloalkenyl, —SC₂₋₃alkynylenearyl,—SC₂₋₃alkynyleneheterocyclyl, —SC₂₋₃alkynyleneheteroaryl,—SC₁₋₃alkylenecycloalkylaryl, —SO₂cycloalkyl, —SO₂cycloalkenyl,—SO₂aryl, —SO₂heterocyclyl, —SO₂heteroaryl, —SO₂C₁₋₃alkylenecycloalkyl,—SO₂C₁₋₃alkylenecycloalkenyl, —SO₂C₁₋₃alkylenearyl,—SO₂C₁₋₃alkyleneheterocyclyl, —SO₂C₁₋₃alkylerleheterOaryl,—SO₂C₂₋₃alkenylenecycloalkyl, —SO₂C₂₋₃alkenylene cycloalkenyl,—SO₂C₂₋₃alkenylenearyl, —SO₂C₂₋₃alkenyleneheterocyclyl,—SO₂C₂₋₃alkenyleneheteroaryl, —SO₂C₂₋₃alkynylenecycloalkyl,—SO₂C₂₋₃alkynylenecycloalkenyl, —SO₂C₂₋₃alkynylenearyl,—SO₂C₂₋₃alkynyieneheterocyclyl, —SO₂C₂₋₃alkynyleneheteroaryl,—SO₂C₁₋₃alkylenecycloalkylaryl, —NHC₁₋₈alkyl, —NHC₂₋₈alkenyl,—NHC₂₋₈alkynyl, —NHcycloalkyl, —NHcycloalkenyl, —NHaryl,—NHheterocyclyl, —NHheteroaryl, —NHC₁₋₃alkylenecycloalkyl,—NHC₁₋₃alkylenecycloalkenyl, —NHC₁₋₃alkylenearyl,—NHC₁₋₃alkyleneheterocyclyl, —NHC₁₋₃alkyleneheteroaryl,—NHC₂₋₃alkenylenecycloalkyl, —NHC₂₋₃alkenylenecycloalkenyl,—NHC₂₋₃alkenylenearyl, —NHC₂₋₃alkenyleneheterocyclyl,—NHC₂₋₃alkenyleneheteroaryl, —NHC₂₋₃alkynylenecycloalkyl,—NHC₂₋₃alkynylenecycloalkenyl, —NHC₂₋₃alkynylenearyl,—NHC₂₋₃alkynyleneheterocyclyl, —NHC₂₋₃alkynyleneheteroaryl,—NHC(═O)cycloalkyl, —NHC(═O)cycloalkenyl, —NHC(═O)aryl,—NHC(═O)heterocyclyl, —NHC(═O)heteroaryl,—NHC(═O)C₁₋₃alkylenecycloalkyl, —NHC(═O)C₁₋₃alkylenecycloalkenyl,—NHC(═O)C₁₋₃alkylenearyl, —NHC(═O)C₁₋₃alkyleneheterocyclyl,—NHC(═O)C₁₋₃alkyleneheteroaryl, —NHC(═O)C₂₋₃alkenylenecycloalkyl,—NHC(═O)C₂₋₃alkenylenecycloalkenyl, —NHC(═O)C₂₋₃alkenylenearyl,—NHC(═O)C₂₋₃alkenyleneheterocyclyl, —NHC(═O)C₂₋₃alkenyleneheteroaryl,—NHC(═O)C₂₋₃alkynylenecycloalkyl, —NHC(═O)C₂₋₃alkynylenecycloalkenyl,—NHC(═O)C₂₋₃alkynylenearyl, —NHC(═O)C₂₋₃alkynyleneheterocyclyl,—NHC(═O)C₂₋₃alkynyleneheteroaryl, —N(CH₃)C₁₋₈alkyl, —N(CH₃)C₂₋₈alkenyl,—N(CH₃)C₂₋₈alkynyl, —N(CH₃)cycloalkyl, —N(CH₃)cycloalkenyl, —N(CH₃)aryl,—N(CH₃)heterocyclyl, —N(CH₃)heteroaryl, —N(CH₃)C₁₋₃alkylenecycloalkyl,—N(CH₃)C₁₋₃alkylenecycloalkenyl, —N(CH₃)C₁₋₃alkylenearyl,—N(CH₃)C₁₋₃alkyleneheterocyclyl, —N(CH₃)C₁₋₃alkyleneheteroaryl,—N(CH₃)C₂₋₃alkenylenecycloalkyl, —N(CH₃)C₂₋₃alkenylenecycloalkenyl,—N(CH₃)C₂₋₃alkenylenearyl, —N(CH₃)C₂₋₃alkenyleneheterocyclyl,—N(CH₃)C₂₋₃alkenyleneheteroaryl, —N(CH₃)C₂₋₃alkynylenecycloalkyl,—N(CH₃)C₂₋₃alkynylenecycloalkenyl, —N(CH₃)C₂₋₃alkynylenearyl,—N(CH₃)C₂₋₃alkynyleneheterocyclyl, —N(CH₃)C₂₋₃alkynyleneheteroaryl,—N(CH₃)C(═O)cycloalkyl, —N(CH₃)C(═O)cycloalkenyl, —N(CH₃)C(═O)aryl,—N(CH₃)C(═O)heterocyclyl, —N(CH₃)C(═O)heteroaryl,—N(CH₃)C(═O)C₁₋₃alkylenecycloalkyl,—N(CH₃)C(═O)C₁₋₃alkylenecycloalkenyl, —N(CH₃)C(═O)C₁₋₃alkylenearyl,—N(CH₃)C(═O)C₁₋₃alkyleneheterocyclyl,—N(CH₃)C(═O)C₁₋₃alkyleneheteroaryl,—N(CH₃)C(═O)C₂₋₃alkenylenecycloalkyl,—N(CH₃)C(═O)C₂₋₃alkenylenecycloalkenyl, —N(CH₃)C(═O)C₂₋₃alkenylenearyl,—N(CH₃)C(═O)C₂₋₃alkenyleneheterocyclyl,—N(CH₃)C(═O)C₂₋₃alkenyleneheteroaryl,—N(CH₃)C(═O)C₂₋₃alkynylenecycloalkyl,—N(CH₃)C(═O)C₂₋₃alkynylenecycloalkenyl, —N(CH₃)C(═O)C₂₋₃alkynylenearyl,—N(CH₃)C(═O)C₂₋₃alkynyleneheterocyclyl,—N(CH₃)C(═O)C₂₋₃alkynyleneheteroaryl, —N(C(═O)CH₃)cycloalkyl,—N(C(═O)CH₃)cycloalkenyl, —N(C(═O)CH₃)aryl, —N(C(═O)CH₃)heterocyclyl,—N(C(═O)CH₃)heteroaryl, —N(C(═O)CH₃)C₁₋₃alkylenecycloalkyl,—N(C(═O)CH₃)C₁₋₃alkylenecycloalkenyl, —N(C(═O)CH₃)C₁₋₃alkylenearyl,—N(C(═O)CH₃)C₁₋₃alkyleneheterocyclyl,—N(C(═O)CH₃)C₁₋₃alkyleneheteroaryl,—N(C(═O)CH₃)C₂₋₃alkenylenecycloalkyl,—N(C(═O)CH₃)C₂₋₃alkenylenecycloalkenyl, —N(C(═O)CH₃)C₂₋₃alkenylenearyl,—N(C(═O)CH₃)C₂₋₃alkenyleneheterocyclyl,—N(C(═O)CH₃)C₂₋₃alkenyleneheteroaryl,—N(C(═O)CH₃)C₂₋₃alkynylenecycloalkyl,—N(C(═O)CH₃)C₂₋₃alkynylenecycloalkenyl, —N(C(═O)CH₃)C₂₋₃alkynylenearyl,—N(C(O)CH₃)C₂₋₃alkynyleneheterocyclyl,—N(C(O)CH₃)C₂₋₃alkynyleneheteroaryl, —N(SO₂CH₃)cycloalkyl,—N(SO₂CH₃)cycloalkenyl, —N(SO₂CH₃)aryl, —N(SO₂CH₃)heterocyclyl,—N(SO₂CH₃)heteroaryl, —N(SO₂CH₃)C₁₋₃alkylenecycloalkyl,—N(SO₂CH₃)C₁₋₃alkylenecycloalkenyl, —N(SO₂CH₃)C₁₋₃alkylenearyl,—N(SO₂CH₃)C₁₋₃alkyleneheterocyclyl, —N(SO₂CH₃)C₁₋₃alkyleneheteroaryl,—N(SO₂CH₃)C₂₋₃alkenylenecycloalkyl,—N(SO₂CH₃)C₂₋₃alkenylenecycloalkenyl, —N(SO₂CH₃)C₂₋₃alkenylenearyl,—N(SO₂CH₃)C₂₋₃alkenyleneheterocyclyl,—N(SO₂CH₃)C₂₋₃alkenyleneheteroaryl, —N(SO₂CH₃)C₂₋₃alkynylenecycloalkyl,—N(SO₂CH₃)C₂₋₃alkynylenecycloalkenyl, —N(SO₂CH₃)C₂₋₃alkynylenearyl,—N(SO₂CH₃)C₂₋₃alkynyleneheterocyclyl,—N(SO₂CH₃)C₂₋₃alkynyleneheteroaryl, —N(CH₂CF₃)cycloalkyl,—N(CH₂CF₃)cycloalkenyl, —N(CH₂CF₃)aryl, —N(CH₂CF₃)heterocyclyl,—N(CH₂CF₃)heteroaryl, —N(CH₂CF₃)C₁₋₃alkylenecycloalkyl,—N(CH₂CF₃)C₁₋₃alkylenecycloalkenyl, —N(CH₂CF₃)C₁₋₃alkylenearyl,—N(CH₂CF₃)C₁₋₃alkyleneheterocyclyl, —N(CH₂CF₃)C₁₋₃alkyleneheteroaryl,—N(CH₂CF₃)C₂₋₃alkenylenecycloalkyl,—N(CH₂CF₃)C₂₋₃alkenylenecycloalkenyl, —N(CH₂CF₃)C₂₋₃alkenylenearyl,—N(CH₂CF₃)C₂₋₃alkenyleneheterocyclyl,—N(CH₂CF₃)C₂₋₃alkenyleneheteroaryl, —N(CH₂CF₃)C₂₋₃alkynylenecycloalkyl,—N(CH₂CF₃)C₂₋₃alkynylenecycloalkenyl, —N(CH₂CF₃)C₂₋₃alkynylenearyl,—N(CH₂CF₃)C₂₋₃alkynyleneheterocyclyl, —N(CH₂CF₃)C₂₋₃alkynyleneheteroaryl, —OCH₂CH(phenyl)CH₂(phenyl), —OCH₂C(phenyl)=CH(phenyl),—CH₂C(═O)NHCH₂cycloalkyl, —CH₂C(═O)NHCH₂cycloalkenyl,—CH₂C(═O)NHCH₂aryl, —CH₂C(═O)NHCH₂heterocyclyl,—CH₂C(═O)NHCH₂heteroaryl, —C(═O)NHC₁₋₃alkylenecycloalkyl,—C(═O)NHC₁₋₃alkylenecycloalkenyl, —C(═O)NHC₁₋₃alkylenearyl,—C(═O)NHC₁₋₃alkyleneheterocyclyl, —C(═O)NHC₁₋₃alkyleneheteroaryl,—CH₂SO₂C₀₋₃alkylenecycloalkyl, —CH₂SO₂C₀₋₃alkylenecycloalkenyl,—CH₂SO₂C₀₋₃alkylenearyl, —CH₂SO₂C₀₋₃alkyleneheterocyclyl,—CH₂SO₂C₀₋₃alkyleneheteroaryl, —CH₂OC₁₋₃alkylenecycloalkyl,—CH₂OC₁₋₃alkylenecycloalkenyl, —CH₂OC₁₋₃alkylenearyl,—CH₂OC₁₋₃alkyleneheterocyclyl, —CH₂OC₁₋₃alkyleneheteroaryl,—CH₂SC₁₋₃alkylenecycloalkyl, —CH₂SC₁₋₃alkylenecycloalkenyl,—CH₂SC₁₋₃alkylenearyl, —CH₂SC₁₋₃alkyleneheterocyclyl,—CH₂SC₁₋₃alkyleneheteroaryl, —CH₂SC₂₋₃alkenylenecycloalkyl,—CH₂SC₂₋₃alkenylenecycloalkenyl, —CH₂SC₂₋₃alkenylenearyl,—CH₂SC₂₋₃alkenyleneheterocyclyl, —CH₂SC₂₋₃alkenyleneheteroaryl,—CH₂SC₂₋₃alkynylenecycloalkyl, —CH₂SC₂₋₃alkynylenecycloalkenyl,—CH₂SC₂₋₃alkynylenearyl, —CH₂SC₂₋₃alkynyleneheterocyclyl,—CH₂SC₂₋₃alkynyleneheteroaryl or —NHC(═O)N(aryl)₂, especially—OCH₂phenyl, —CH₂Ophenyl, —OCH₂CH₂phenyl, —OCH₂CH₂CH₂phenyl,—OCH₂CH₂CH₂-(4-fluorophenyl), —CH₂CH═CHphenyl, —OCH₂CH═CHphenyl,—C=CCH₂CH₂phenyl, ═CHC(═O)NHCH₂phenyl, —OCH₂cyclopropyl,—OCH₂-(2-phenyl)cyclopropyl, —OCH₂-4-oxazole,—CH₂-4-(3-methyl-2-phenyl)oxazole, -1-azetidine,-1-(3-benzyloxy)azetidine, -1-(3-phenyl)azetidine, —N(CH₃)(CH₂CH₂CH₃),—N(CH₃)(CH₂CH₂CH₂C(CH₃)₃), —N(CH₃)(CH₂C≡CH), —N(CH₃)(CH₂C≡CC(CH₃)₃),—N(CH₃)CH₂CH₂CH₂phenyl, —N(CH₂CF₃)CH₂CH₂CH₂-(4-fluorophenyl),—N(CH₃)CH₂CH₂phenyl, —N(CH₃)CH₂CH₂CH₂-(4-fluorophenyl),—N(CH₃)CH₂CH₂(4-fluorophenyl), —N(CH₃)CH₂CH₂O-(4-fluorophenyl),—N(CH₃)CH₂C≡C-(3-methyl-4-methoxyphenyl), -1-piperazine,-1-(4-phenyl)piperazine, -1-(4-benzyl)piperazine,-1-(3-benzyl)piperazine, -1-(4-methyl-3-phenyl)piperazine,-4-morpholine, -4-(2-phenyl)morpholine, -4-(2-benzyl)morpholine,-4-(3-benzyl)morpholine, —N(CH₃)cyclopropyl,—N(CH₃)-(2-phenyl)cyclopropyl, —OCH₂C(phenyl)=CH(phenyl),—OCH₂CH(phenyl)CH₂(phenyl), —Ophenyl, —O-(4-benzyloxy)phenyl,—O-(3-benzyloxy)phenyl, —O-(2-benzyloxy)phenyl, —O-(4-phenoxy)phenyl,—O-(3-phenoxy)phenyl, —O-(2-phenoxy)phenyl; —OCH₂—C≡Cphenyl,—CH₂C(═O)NHCH₂phenyl, —C(═O)NHCH₂phenyl, —C(═O)NHCH₂CH₂phenyl,—NHCH₂CH₂CH₂phenyl, —NHCH₂CH₂phenyl, —CH₂CH₂CH₂phenyl,—CH₂CH₂CH₂CH₂phenyl, —CH₂OCH₂phenyl, —CH₂Ophenyl, -1-piperidine,-1-(4-phenyl)piperidine, -1-(3-phenyl)piperidine,-1-(3-benzyl)piperidine, -2-(phenyl)pyrrolidine, -3-(phenyl)pyrrolidine,—CH₂OCH₂CH₂phenyl, —CH₂CH₂OCH₂phenyl, -2-oxazole, -2-(5-phenyl)oxazole,-2-(5-benzyl)oxazole, —CH₂SO₂CH₂CH₂phenyl, -1-pyrrolidine,-1-(2-benzyl)pyrrolidine, —N(CH₃)CH₂cyclopropyl,—N(CH₃)CH₂-(2-phenyl)cyclopropyl, —N(CH₃)(CH₂)₃phenyl,—N(CH₃)(CH₂)₃(4-fluorophenyl), —N(CH₃)(CH₂)₃(4-methoxy-3-methylphenyl),—N(CH₃)(CH₂)₄phenyl, —N(CH₃)(CH₂)₃pyridine, —NHC(═O)N(phenyl)(phenyl),—OCH₂-4-oxazole, —OCH₂-4-(2-phenyl)oxazole, —O-4-oxazole,—O-4-(2-phenyl)oxazole, —NHC(═O)CH═CHphenyl, —N(CH₃)C(═O)CH═CHphenyl,—NHC(O)CH₂CH₂phenyl, —N(CH₃)C(═O)CH₂CH₂phenyl,—N(C(═O)CH₃)CH₂CH₂CH₂phenyl, N(SO₂CH₃)CH₂CH₂CH₂phenyl, —CH₂SO₂CH₂phenyl,—CH₂SO₂phenyl, —CH₂SCH₂CH₂phenyl, —CH₂SCH₂phenyl, —CH₂Sphenyl,—CH₂SCH₂CH₂CH₂phenyl, —SO₂CH₂CH₂CH₂phenyl, —SCH₂CH₂phenyl,—SO₂CH₂CH₂phenyl, —SCH₂CH₂-(4-fluorophenyl),—SO₂CH₂CH₂CH₂-(4-fluorophenyl), -1-(5-phenyl-1,2,3-triazolyl),-1-(5-benzyl-1,2,3-triazolyl), -4-(5-benzyl-3-oxo-morpholinyl),-2-(3-phenylthiophenyl), -2-(4-phenyl-1,3-thiazolyl),

R^(2b) is hydrogen,

R³ is —CO₂H, —CH₂CO₂H, —C(═O)C(═O)OH, —C(═O)NHSO₂C₁₋₆alkyl,—C(═O)NHSO₂N(C₁₋₆alkyl)₂, —C(═O)NHSO₂phenyl, —C(═O)NHSO₂CF₃, —SO₃H,PO₃H₂, tetrazolyl, —CH₂NHSO₂C₁₋₆alkyl, —CH₂OH, —C(═O)NH₂ or CN,especially —CO₂H, —CH₂CO₂H, —CH₂OH, —C(═O)NHSO₂C₁₋₄alkyl,—C(═O)NHSO₂N(C₁₋₃alkyl)₂, —C(═O)NHSO₂phenyl, tetrazolyl,—CH₂NHSO₂(C₁₋₄alkyl), —C(═O)NH₂ or CN, —C(═O)NHSO₂CF₃, more especially—CO₂H;

R⁴ is hydrogen or R³ and R⁴ together form:

especially where R⁴ is hydrogen;

R⁵ is hydrogen or together with R² forms an aryl, heteroaryl orheterocyclyl ring selected from:

where* indicates the fused bond, and R is selected from —C₁₋₃alkyl,—OC₁₋₃alkyl, —OCF₃, —OCHF₂, —OCH₂phenyl, —CH═CHphenyl, —CH₂CH₂phenyl,—CH(OH)CH(OH)phenyl, —SO₂NHphenyl, —NHSO₂phenyl, —NHC(O)NHphenyl,—NHC(O)Ophenyl, —CH₂phenyl, —Ophenyl, —OCH₂CH═CHphenyl, —OCH₂CH₂phenyl,—OCH₂CH₂CH₂phenyl and -phenyl;

R⁶ and R⁷ are independently selected from phenyl and cyclohexyl,especially where both R⁶ and R⁷ are phenyl;

R⁸ is hydrogen, methyl, ethyl or phenyl.

In some embodiments, especially when R³ appears on the carbon atom of Ythat is adjacent in the ring to the ring nitrogen, R³ has an Sstereochemistry.

In some embodiments, R² and R³ are cis relative to one another, that is,they are positioned on the same face of the N-containing 4- or5-membered ring.

In some embodiments, the group R² contains at least one stereocentre. Inembodiments where R² comprises a cyclohexyl or 6-membered heterocyclylring, substituted in the position adjacent to the attachment to theazetidine or pyrrolidine ring, one stereoisomer may be preferred overthe other stereoisomer.

In one embodiment, the compound of formula (I) is a compound of formula(II):

wherein X is absent and Y is —CHR³CHR⁴CH₂—, —CH₂CHR³CHR⁴— or—CH₂CH₂CHR³— or X is —CHR⁵— and Y is —CHR³—, —CHR³CHR⁴—, —CHR³CR⁴═,—CH₂CHR³—, —CR³═CH— or —CH═CR³—, wherein when Y is —CHR³CR⁴═, R^(2b) isabsent; or

X is —CH₂CH⁵— and Y is —CHR³— and

R¹, R², R³, R⁴ and R⁵ are as defined for formula (I).

In particular embodiments of compound of formula (II): R¹ is—C(═O)CH(phenyl)(phenyl), —C(═O)CH(phenyl)(cycloalkyl),—C(═O)CH(cycloalkyl)(cycloalkyl), —C(═O)N(phenyl)(phenyl),—C(═O)N(phenyl)(cycloalkyl) or —C(═O)N(cycloalkyl)(cycloalkyl),especially —C(═O)CH(phenyl)(phenyl) or —C(═O)N(phenyl)(phenyl);

R² is cycloalkyl, cycloalkenyl, aryl, heterocyclyl, heteroaryl,-heterocyclylaryl, -heterocyclyl C₁₋₃alkylenearyl,—C₁₋₄alkylenecycloalkyl, —C₁₋₄alkylenecycloalkenyl, —C₁₋₄alkylenearyl,—C₁₋₄alkyleneheterocyclyl, —C₁₋₄alkyleneheteroaryl,—C₂₋₄alkenylenecycloalkyl, —C₂₋₄alkenylenecycloalkenyl,—C₂₋₄alkenylenearyl, —C₂₋₄alkenyleneheterocyclyl,—C₂₋₄alkenyleneheteroaryl, —C₂₋₄alkynylenecycloalkyl,—C₂₋₄alkynylenecycloalkenyl, —C₂₋₄alkynylenearyl,—C₂₋₄alkynyleneheterocyclyl, —C₂₋₄alkynyleneheteroaryl,═CHC(═O)NHCH₂cycloalkyl, ═CHC(═O)NHCH₂cycloalkenyl, ═CHC(═O)NHCH₂aryl,═CHC(═O)NHCH₂heterocyclyl, ═CHC(═O)NHCH₂heteroaryl, —Ocycloalkyl,—Ocycloalkenyl, —Oaryl, —Oheterocyclyl, —Oheteroaryl,—OC₁₋₃alkylenecycloalkyl, —OC₁₋₃alkylenecycloalkenyl,—OC₁₋₃alkylenearyl, —OC₁₋₃alkyleneheterocyclyl,—OC₁₋₃alkyleneheteroaryl, —OC₂₋₃alkenylenecycloalkyl,—OC₂₋₃alkenylenecycloalkenyl, —OC₂₋₃alkenylenearyl,—OC₂₋₃alkenyleneheterocyclyl, —OC₂₋₃alkenyleneheteroaryl,—OC₂₋₃alkynylenecycloalkyl, —OC₂₋₃alkynylenecycloalkenyl,—OC₂₋₃alkynylenearyl, —OC₂₋₃alkynyleneheterocyclyl,—OC₂₋₃alkynyleneheteroaryl, —OC₁₋₃alkylenecycloalkylaryl, —OarylOaryl,—OarylOC₁₋₃alkylenearyl, —Scycloalkyl, —Scycloalkenyl, —Saryl,—Sheterocyclyl, —Sheteroaryl, —SC₁₋₃alkylenecycloalkyl,—SC₁₋₃alkylenecycloalkenyl, —SC₁₋₃alkylenearyl,—SC₁₋₃alkyleneheterocyclyl, —SC₁₋₃alkyleneheteroaryl,—SC₂₋₃alkenylenecycloalkyl, —SC₂₋₃alkenylenecycloalkenyl,—SC₂₋₃alkenylenearyl, —SC₂₋₃alkenyleneheterocyclyl,—SC₂₋₃alkenyleneheteroaryl, —SC₂₋₃alkynylenecycloalkyl,—SC₂₋₃alkynylenecycloalkenyl, —SC₂₋₃alkynylenearyl,—SC₂₋₃alkynyleneheterocyclyl, —SC₂₋₃alkynyleneheteroaryl,—SC₁₋₃alkylenecycloalkylaryl, —SO₂cycloalkyl, —SO₂cycloalkenyl,—SO₂aryl, —SO₂heterocyclyl, —SO₂heteroaryl, —SO₂C₁₋₃alkylenecycloalkyl,—SO₂C₁₋₃alkylenecycloalkenyl, —SO₂C₁₋₃alkylenearyl,—SO₂C₁₋₃alkyleneheterocyclyl, —SO₂C₁₋₃alkyleneheteroaryl,—SO₂C₂₋₃alkenylenecycloalkyl, —SO₂C₂₋₃alkenylenecycloalkenyl,—SO₂C₂₋₃alkenylenearyl, —SO₂C₂₋₃alkenyleneheterocyclyl,—SO₂C₂₋₃alkenyleneheteroaryl, —SO₂C₂₋₃alkynylenecycloalkyl,—SO₂C₂₋₃alkynylenecycloalkenyl, —SO₂C₂₋₃alkynylenearyl,—SO₂C₂₋₃alkynyleneheterocyclyl, —SO₂C₂₋₃alkynyleneheteroaryl,—SO₂C₁₋₃alkylenecycloalkylaryl, —NHC₁₋₈alkyl, —NHC₂₋₈alkenyl,—NHC₂₋₈alkynyl, —NHcycloalkyl, —NHcycloalkenyl, —NHaryl,—NHheterocyclyl, —NHheteroaryl, —NHC₁₋₃alkylenecycloalkyl,—NHC₁₋₃alkylenecycloalkenyl, —NHC₁₋₃alkylenearyl,—NHC₁₋₃alkyleneheterocyclyl, —NHC₁₋₃alkyleneheteroaryl,—NHC₂₋₃alkenylenecycloalkyl, —NHC₂₋₃alkenylenecycloalkenyl,—NHC₂₋₃alkenylenearyl, —NHC₂₋₃alkenyleneheterocyclyl,—NHC₂₋₃alkenyleneheteroaryl, —NHC₂₋₃alkynylenecycloalkyl,—NHC₂₋₃alkynylenecycloalkenyl, —NHC₂₋₃alkynylenearyl,—NHC₂₋₃alkynyleneheterocyclyl, —NHC₂₋₃alkynyleneheteroaryl,—NHC(═O)cycloalkyl, —NHC(═O)cycloalkenyl, —NHC(═O)aryl,—NHC(═O)heterocyclyl, —NHC(═O)heteroaryl,—NHC(═O)C₁₋₃alkylenecycloalkyl, —NHC(═O)C₁₋₃alkylenecycloalkenyl,—NHC(═O)C₁₋₃alkylenearyl, —NHC(═O)C₁₋₃alkyleneheterocyclyl,—NHC(═O)C₁₋₃alkyleneheteroaryl, —NHC(═O)C₂₋₃alkenylenecycloalkyl,—NHC(═O)C₂₋₃alkenylenecycloalkenyl, —NHC(═O)C₂₋₃alkenylenearyl,—NHC(═O)C₂₋₃alkenyleneheterocyclyl, —NHC(═O)C₂₋₃alkenyleneheteroaryl,—NHC(═O)C₂₋₃alkynylenecycloalkyl, —NHC(═O)C₂₋₃alkynylenecycloalkenyl,—NHC(═O)C₂₋₃alkynylenearyl, —NHC(═O)C₂₋₃alkynyleneheterocyclyl,—NHC(═O)C₂₋₃alkynyleneheteroaryl, —N(CH₃)C₁₋₈alkyl, —N(CH₃)C₂₋₈alkenyl,—N(CH₃)C₂₋₈alkynyl, —N(CH₃)cycloalkyl, —N(CH₃)cycloalkenyl, —N(CH₃)aryl,—N(CH₃)heterocyclyl, —N(CH₃)heteroaryl, —N(CH₃)C₁₋₃alkylenecycloalkyl,—N(CH₃)C₁₋₃alkylenecycloalkenyl, —N(CH₃)C₁₋₃alkylenearyl,—N(CH₃)C₁₋₃alkyleneheterocyclyl, —N(CH₃)C₁₋₃alkyleneheteroaryl,—N(CH₃)C₂₋₃alkenylenecycloalkyl, —N(CH₃)C₂₋₃alkenylenecycloalkenyl,—N(CH₃)C₂₋₃alkenylenearyl, —N(CH₃)C₂₋₃alkenyleneheterocyclyl,—N(CH₃)C₂₋₃alkenyleneheteroaryl, —N(CH₃)C₂₋₃alkynylenecycloalkyl,—N(CH₃)C₂₋₃alkynylenecycloalkenyl, —N(CH₃)C₂₋₃alkynylenearyl,—N(CH₃)C₂₋₃alkynyleneheterocyclyl, —N(CH₃)C₂₋₃alkynyleneheteroaryl,—N(CH₃)C(═O)cycloalkyl, —N(CH₃)C(═O)cycloalkenyl, —N(CH₃)C(═O)aryl,—N(CH₃)C(═O)heterocyclyl, —N(CH₃)C(═O)heteroaryl,—N(CH₃)C(═O)C₁₋₃alkylenecycloalkyl,—N(CH₃)C(═O)C₁₋₃alkylenecycloalkenyl, —N(CH₃)C(═O)C₁₋₃alkylenearyl,—N(CH₃)C(═O)C₁₋₃alkyleneheterocyclyl,—N(CH₃)C(═O)C₁₋₃alkyleneheteroaryl,—N(CH₃)C(═O)C₂₋₃alkenylenecycloalkyl,—N(CH₃)C(═O)C₂₋₃alkenylenecycloalkenyl, —N(CH₃)C(═O)C₂₋₃alkenylenearyl,—N(CH₃)C(═O)C₂₋₃alkenyleneheterocyclyl,—N(CH₃)C(═O)C₂₋₃alkenyleneheteroaryl,—N(CH₃)C(═O)C₂₋₃alkynylenecycloalkyl,—N(CH₃)C(═O)C₂₋₃alkynylenecycloalkenyl, —N(CH₃)C(═O)C₂₋₃alkynylenearyl,—N(CH₃)C(═O)C₂₋₃alkynyleneheterocyclyl,—N(CH₃)C(═O)C₂₋₃alkynyleneheteroaryl, —N(C(═O)CH₃)cycloalkyl,—N(C(═O)CH₃)cycloalkenyl, —N(C(═O)CH₃)aryl, —N(C(═O)CH₃)heterocyclyl,—N(C(═O)CH₃)heteroaryl, —N(C(═O)CH₃)C₁₋₃alkylenecycloalkyl,—N(C(═O)CH₃)C₁₋₃alkylenecycloalkenyl, —N(C(═O)CH₃)C₁₋₃alkylenearyl,—N(C(═O)CH₃)C₁₋₃alkyleneheterocyclyl,—N(C(═O)CH₃)C₁₋₃alkyleneheteroaryl,—N(C(═O)CH₃)C₂₋₃alkenylenecycloalkyl,—N(C(═O)CH₃)C₂₋₃alkenylenecycloalkenyl, —N(C(═O)CH₃)C₂₋₃alkenylenearyl,—N(C(═O)CH₃)C₂₋₃alkenyleneheterocyclyl,—N(C(═O)CH₃)C₂₋₃alkenyleneheteroaryl,—N(C(═O)CH₃)C₂₋₃alkynylenecycloalkyl,—N(C(═O)CH₃)C₂₋₃alkynylenecycloalkenyl, —N(C(═O)CH₃)C₂₋₃alkynylenearyl,—N(C(O)CH₃)C₂₋₃alkynyleneheterocyclyl,—N(C(O)CH₃)C₂₋₃alkynyleneheteroaryl, —N(SO₂CH₃)cycloalkyl,—N(SO₂CH₃)cycloalkenyl, —N(SO₂CH₃)aryl, —N(SO₂CH₃)heterocyclyl,—N(SO₂CH₃)heteroaryl, —N(SO₂CH₃)C₁₋₃alkylenecycloalkyl,—N(SO₂CH₃)C₁₋₃alkylenecycloalkenyl, —N(SO₂CH₃)C₁₋₃alkylenearyl,—N(SO₂CH₃)C₁₋₃alkyleneheterocyclyl, —N(SO₂CH₃)C₁₋₃alkyleneheteroaryl,—N(SO₂CH₃)C₂₋₃alkenylenecycloalkyl,—N(SO₂CH₃)C₂₋₃alkenylenecycloalkenyl, —N(SO₂CH₃)C₂₋₃alkenylenearyl,—N(SO₂CH₃)C₂₋₃alkenyleneheterocyclyl,—N(SO₂CH₃)C₂₋₃alkenyleneheteroaryl, —N(SO₂CH₃)C₂₋₃alkynylenecycloalkyl,—N(SO₂CH₃)C₂₋₃alkynylenecycloalkenyl, —N(SO₂CH₃)C₂₋₃alkynylenearyl,—N(SO₂CH₃)C₂₋₃alkynyleneheterocyclyl,—N(SO₂CH₃)C₂₋₃alkynyleneheteroaryl, —N(CH₂CF₃)cycloalkyl,—N(CH₂CF₃)cycloalkenyl, —N(CH₂CF₃)aryl, —N(CH₂CF₃)heterocyclyl,—N(CH₂CF₃)heteroaryl, —N(CH₂CF₃)C₁₋₃alkylenecycloalkyl,—N(CH₂CF₃)C₁₋₃alkylenecycloalkenyl, —N(CH₂CF₃)C₁₋₃alkylenearyl,—N(CH₂CF₃)C₁₋₃alkyleneheterocyclyl, —N(CH₂CF₃)C₁₋₃alkyleneheteroaryl,—N(CH₂CF₃)C₂₋₃alkenylenecycloalkyl,—N(CH₂CF₃)C₂₋₃alkenylenecycloalkenyl, —N(CH₂CF₃)C₂₋₃alkenylenearyl,—N(CH₂CF₃)C₂₋₃alkenyleneheterocyclyl,—N(CH₂CF₃)C₂₋₃alkenyleneheteroaryl, —N(CH₂CF₃)C₂₋₃alkynylenecycloalkyl,—N(CH₂CF₃)C₂₋₃alkynylenecycloalkenyl, —N(CH₂CF₃)C₂₋₃alkynylenearyl,—N(CH₂CF₃)C₂₋₃alkynyleneheterocyclyl,—N(CH₂CF₃)C₂₋₃alkynyleneheteroaryl, —OCH₂CH(phenyl)CH₂(phenyl),—OCH₂C(phenyl)=CH(phenyl), —CH₂C(═O)NHCH₂cycloalkyl,—CH₂C(═O)NHCH₂cycloalkenyl, —CH₂C(═O)NHCH₂aryl,—CH₂C(═O)NHCH₂heterocyclyl, —CH₂C(═O)NHCH₂heteroaryl,—C(═O)NHC₁₋₃alkylenecycloalkyl, —C(═O)NHC₁₋₃alkylenecycloalkenyl,—C(═O)NHC₁₋₃alkylenearyl, —C(═O)NHC₁₋₃alkyleneheterocyclyl,—C(═O)NHC₁₋₃alkyleneheteroaryl, —CH₂SO₂C₀₋₃alkylenecycloalkyl,—CH₂SO₂C₀₋₃alkylenecycloalkenyl, —CH₂SO₂C₀₋₃alkylenearyl,—CH₂SO₂C₀₋₃alkyleneheterocyclyl, —CH₂SO₂C₀₋₃alkyleneheteroaryl,—CH₂OC₁₋₃alkylenecycloalkyl, —CH₂OC₁₋₃alkylenecycloalkenyl,—CH₂OC₁₋₃alkylenearyl, —CH₂OC₁₋₃alkyleneheterocyclyl,—CH₂OC₁₋₃alkyleneheteroaryl, —CH₂SC₁₋₃alkylenecycloalkyl,—CH₂SC₁₋₃alkylenecycloalkenyl, —CH₂SC₁₋₃alkylenearyl,—CH₂SC₁₋₃alkyleneheterocyclyl, —CH₂SC₁₋₃alkyleneheteroaryl,—CH₂SC₂₋₃alkenylenecycloalkyl, —CH₂SC₂₋₃alkenylenecycloalkenyl,—CH₂SC₂₋₃alkenylenearyl, —CH₂SC₂₋₃alkenyleneheterocyclyl,—CH₂SC₂₋₃alkenyleneheteroaryl, —CH₂SC₂₋₃alkynylenecycloalkyl,—CH₂SC₂₋₃alkynylenecycloalkenyl, —CH₂SC₂₋₃alkynylenearyl,—CH₂SC₂₋₃alkynyleneheterocyclyl, —CH₂SC₂₋₃alkynyleneheteroaryl or—NHC(═O)N(aryl)₂, especially —OCH₂phenyl, —CH₂Ophenyl, —OCH₂CH₂phenyl,—OCH₂CH₂CH₂phenyl, —OCH₂CH₂CH₂-(4-fluorophenyl), —CH₂CH═CHphenyl,—OCH₂CH═CHphenyl, —C≡CCH₂CH₂phenyl, ═CHC(═O)NHCH₂phenyl,—OCH₂cyclopropyl, —OCH₂-(2-phenyl)cyclopropyl, —OCH₂-4-oxazole,—CH₂-4-(3-methyl-2-phenyl)oxazole, -1-azetidine,-1-(3-benzyloxy)azetidine, -1-(3-phenyl)azetidine, —N(CH₃)(CH₂CH₂CH₃),—N(CH₃)(CH₂CH₂CH₂C(CH₃)₃), —N(CH₃)(CH₂C≡CH), —N(CH₃)(CH₂C≡CC(CH₃)₃),—N(CH₃)CH₂CH₂CH₂phenyl,—N(CH₂CF₃)CH₂CH₂CH₂-(4-fluorophenyl)-N(CH₃)CH₂CH₂phenyl,—N(CH₃)CH₂CH₂CH₂-(4-fluorophenyl), —N(CH₃)CH₂C≡Cphenyl,—N(CH₃)CH₂C≡C-(3-methyl-4-methoxyphenyl),—N(CH₃)CH₂CH₂-(4-fluorophenyl), —N(CH₃)CH₂CH₂-(4-fluorophenyl),-1-piperazine, -1-(4-phenyl)piperazine, -1-(4-benzyl)piperazine,-1-(3-benzyl)piperazine, -1-(4-methyl-3-phenyl)piperazine,-4-morpholine, -4-(2-phenyl)morpholine, -4-(2-benzyl)morpholine,-4-(3-benzyl)morpholine, —N(CH₃)cyclopropyl,—N(CH₃)-(2-phenyl)cyclopropyl, —OCH₂C(phenyl)=CH(phenyl),—OCH₂CH(phenyl)CH₂(phenyl), —Ophenyl, —O-(4-benzyloxy)phenyl,—O-(3-benzyloxy)phenyl, —O-(2-benzyloxy)phenyl, —O-(4-phenoxy)phenyl,—O-(3-phenoxy)phenyl, —O-(2-phenoxy)phenyl, —OCH₂—C≡Cphenyl,—CH₂C(═O)NHCH₂phenyl, —C(═O)NHCH₂phenyl, —C(═O)NHCH₂CH₂phenyl,—NHCH₂CH₂CH₂phenyl, —NHCH₂CH₂phenyl, —CH₂CH₂CH₂phenyl,—CH₂CH₂CH₂CH₂phenyl, —CH₂OCH₂phenyl, —CH₂Ophenyl, -1-piperidine,-1-(4-phenyl)piperidine, -1-(3-phenyl)piperidine,-1-(3-benzyl)piperidine, -2-(phenyl)pyrrolidine, -3-(phenyl)pyrrolidine,—CH₂OCH₂CH₂phenyl, —CH₂CH₂OCH₂phenyl, -2-oxazole, -2-(5-phenyl)oxazole,-2-(5-benzyl)oxazole, —CH₂SO₂CH₂CH₂phenyl, -1-pyrrolidine,-1-(2-benzyl)pyrrolidine, —N(CH₃)CH₂cyclopropyl,—N(CH₃)CH₂-(2-phenyl)cyclopropyl, —N(CH₃)(CH₂)₃phenyl,—N(CH₃)(CH₂)₃(4-fluorophenyl), —N(CH₃)(CH₂)₃(4-methoxy-3-methylphenyl),—N(CH₃)(CH₂)₄phenyl, —N(CH₃)(CH₂)₃pyridine, —NHC(═O)N(phenyl)(phenyl),—OCH₂-4-oxazole, —OCH₂-4-(2-phenyl)oxazole, —O-4-oxazole,—O4-(2-phenyl)oxazole, —NHC(═O)CH═CHphenyl, —N(CH₃)C(═O)CH═CHphenyl,—NHC(O)CH₂CH₂phenyl, —N(CH₃)C(═O)CH₂CH₂phenyl,—N(C(═O)CH₃)CH₂CH₂CH₂phenyl, N(SO₂CH₃)CH₂CH₂CH₂phenyl, —CH₂SO₂CH₂phenyl,—CH₂SO₂phenyl, —CH₂SCH₂CH₂phenyl, —CH₂SCH₂phenyl, —CH₂S phenyl,—CH₂SCH₂CH₂CH₂phenyl, —SO₂CH₂CH₂CH₂phenyl, —SCH₂CH₂phenyl,—SO₂CH₂CH₂phenyl, —SCH₂CH₂-(4-fluorophenyl),—SO₂CH₂CH₂CH₂-(4-fluorophenyl), -1-(5-phenyl-1,2,3-triazolyl),-1-(5-benzyl-1,2,3-triazolyl), -4-(5-benzyl-3-oxo-morpholinyl),-2-(3-phenylthiophenyl), -2-(4-phenyl-1,3-thiazolyl),

R^(2b) is hydrogen;

R³ is —CO₂H, —CH₂CO₂H, —CH₂OH, —C(═O)C(═O)OH, —C(═O)NHSO₂C₁₋₆alkyl,—C(═O)NHSO₂N(C₁₋₆alkyl)₂, —C(═O)NHSO₂phenyl, —C(═O)NHSO₂CF₃, —SO₃H,PO₃H₂, tetrazolyl, —CH₂NHSO₂C₁₋₆alkyl, —CH₂OH, —C(═O)NH₂ or —CNespecially —CO₂H, —CH₂CO₂H, —C(═O)NHSO₂C₁₋₄alkyl,—C(═O)NHSO₂(C₁₋₃alkyl)₂, —C(═O)NHSO₂phenyl, tetrazolyl,—CH₂NHSO₂C₁₋₄alkyl, —C(═O)NH₂, CN or —C(═O)NHSO₂CF₃, more especially—CO₂H;

R⁴ is hydrogen or R³ and R⁴ together form:

especially hydrogen;

R⁵ is hydrogen or together with R² forms an aryl, heteroaryl orheterocyclyl ring selected from:

where* indicates the fused bond, and R is selected from —C₁₋₃alkyl,—OC₁₋₃alkyl, —OCF₃, —OCHF₂, —OCH₂phenyl, —CH═CHphenyl, —CH₂CH₂phenyl,—CH(OH)CH(OH)phenyl, —SO₂NHphenyl, —NHSO₂phenyl, —NHC(O)NHphenyl,—NHC(O)Ophenyl, —CH₂phenyl, —Ophenyl, —OCH₂CH═CHphenyl, —OCH₂CH₂phenyl,—OCH₂CH₂CH₂phenyl and -phenyl;

especially where R⁵ and R² together forms one of:

where R is selected from —C₁₋₃alkyl, —OC₁₋₃alkyl, —OCF₃, —OCHF₂,—OCH₂phenyl, —CH═CHphenyl, —CH₂CH₂phenyl, —CH(OH)CH(OH)phenyl,—C≡Cphenyl, —SO₂NHphenyl, —NHSO₂phenyl, —NHC(O)NHphenyl, —NHC(O)Ophenyl,—CH₂phenyl, —Ophenyl, —OCH₂CH═CHphenyl, —OCH₂CH₂phenyl,—OCH₂CH₂CH₂phenyl and -phenyl especially —OCH₂phenyl or —CH₂phenyl;

Particular compounds of formula (II) are:

Rela- Com- tive pound X Y R¹ R² R³ R²/R³ R⁴ R³/R⁴ R⁵ R²/R⁵ 1 —CR⁵——CH═CR³— —C(O)CH (phenyl)₂ — —CO₂H — H — —

2 —CHR⁵— —CHR³CHR⁴— —C(O)CH benzyloxy —CO₂H (S) cis H — H — (phenyl)₂ 3—CHR⁵— —CHR³CHR⁴— —C(O)CH benzyloxy —CO₂H (S) trans H — H — (phenyl)₂ 4—CHR⁵— —CHR³CHR⁴— —C(O)CH phenylCH₂CH₂O— —CO₂H (S) cis H — H — (phenyl)₂5 —CHR⁵— —CHR³CHR⁴— —C(O)CH phenylCH═ —CO₂H (S) cis H — H — (phenyl)₂CHCH₂O— 6 —CHR⁵— —CHR³CHR⁴— —C(O)CH phenylCH₂CH₂ —CO₂H (S) cis H — H —(phenyl)₂ CH₂O— 7 —CHR⁵— —CHR³CHR⁴— —C(O)CH phenylCH₂CH₂O— —CO₂H (S)trans H — H — (phenyl)₂ 8 —CHR⁵— —CHR³CHR⁴— —C(O)CH phenylCH═CHCH₂O——CO₂H (S) trans H — H — (phenyl)₂ 9 —CHR5— —CHR3CHR4— —C(0)CHphenylCH₂CH₂ —CO2H (S) trans H — H — (phenyl)₂ CH₂O— 10 —CHR⁵——CHR³CHR⁴— —C(O)CH ═CHC(O)NHCH₂ —CO₂H (S) — H — H — (phenyl)₂ phenyl 11—CR⁵— —CR³═CH— —C(O)CH (phenyl)₂ — —CO₂H — — — —

12 —CR⁵— —CR³═CH— —C(O)CH (phenyl)₂ — —C(O)C(O)OH — — — H

13 —CR⁵— —CR³═CH— —C(O)N (phenyl)₂ — —CO₂H — — — —

14 —CR⁵— —CH═CR³— —C(O)N (phenyl)₂ — —C(O)C(O)OH — — — —

15 —CR⁵— —CHR³CHR⁴— —C(O)CH (phenyl)₂ — —CO₂H (R/S) — H — —

16 —CHR⁵— —CHR³CHR⁴— —C(O)CH (phenyl)₂

—CO₂H (S) cis H — H 17 —CHR⁵— —CHR³CHR⁴— —C(O)CH (phenyl)₂

—CO₂H (S) cis H — H 18 —CHR⁵— —CHR³CHR⁴— —C(O)CH —OCH₂-(2-phenyl)- —CO₂H(S) cis H — H — (phenyl)₂ 5-methyl)-4-oxazole 19 —CHR⁵— —CHR³CHR⁴——C(O)CH -1-(3-benzyloxy) —CO₂H (S) cis H — H — (phenyl)₂ azetidine 20—CHR⁵— —CHR³CHR⁴— —C(O)CH -1-(3-phenyl) —CO₂H (S) cis H — H — (phenyl)₂azetidine 21 —CHR⁵— —CHR³CHR⁴— —C(O)CH —N(CH₃)CH₂CH₂ —CO₂H (S) cis H — H— (phenyl)₂ CH₂phenyl 22 —CHR⁵— —CHR³CHR⁴— —C(O)CH —N(CH₃)CH₂CH₂ —CO₂H(S) cis H — H — (phenyl)₂ phenyl 23 —CHR⁵— —CHR³CHR⁴— —C(O)CH-1-(4-phenyl)- —CO₂H (S) cis H — H — (phenyl)₂ piperazine 24 —CHR⁵——CHR³CHR⁴— —C(O)CH -1-(4-methyl-3R- —CO₂H (S) cis H — H — (phenyl)₂phenyl)piperazine 25 —CHR⁵— —CHR³CHR⁴— —C(O)CH -1-(4-methyl-3S- —CO₂H(S) cis H — H — (phenyl)₂ phenyl)piperazine 26 —CHR⁵— —CHR³CHR⁴— —C(O)CH-4-(2R-phenyl) —CO₂H (S) cis H — H — (phenyl)₂ morpholine 27 —CHR⁵——CHR³CHR⁴— —C(O)CH -4-(2S-phenyl) —CO₂H (S) cis H — H — (phenyl)₂morpholine 28 —CHR⁵— —CHR³CHR⁴— —C(O)CH -4-(2S-benzyl) —CO₂H (S) cis H —H — (phenyl)₂ morpholine 29 —CHR⁵— —CHR³CHR⁴— —C(O)CH —N(CH₃)-(2-phenyl)—CO₂H (S) cis H — H — (phenyl)₂ cyclopropyl 30 —CHR⁵— —CHR³CHR⁴— —C(O)CH—N(CH₃)-(2-phenyl) —CO₂H (S) cis H — H — (phenyl)₂ Cyclopropyl 31 —CHR⁵——CHR³CHR⁴— —C(O)CH —OCH₂C(phenyl) —CO₂H (S) cis H — H — (phenyl)₂═CH(phenyl) 32 —CHR⁵— —CHR³CHR⁴— —C(O)CH —OCH₂CH(phenyl) —CO₂H (S) cis H— H — (phenyl)₂ CH₂(phenyl) 33 —CHR⁵— —CHR³CHR⁴— —C(O)CH—O-(2-benyzloxy) —CO₂H (S) cis H — H — (phenyl)₂ phenyl 34 —CHR⁵——CHR³CHR⁴— —C(O)CH —O-(3-phenoxy) —CO₂H (S) cis H — H — (phenyl)₂ phenyl35 —CHR⁵— —CHR³CHR⁴— —C(O)CH —O-(2-phenoxy) —CO₂H (S) cis H — H —(phenyl)₂ phenyl 36 —CHR⁵— —CHR³CHR⁴— —C(O)CH —OCH₂C≡C-phenyl —CO₂H (S)cis H — H — (phenyl)₂ 37 —CHR⁵— —CHR³CHR⁴— —C(O)CH —OCH₂CH═CH —CO₂H (R)cis H — H — (phenyl)₂ phenyl 38 —CHR⁵— —CHR³CHR⁴— —C(O)CH —OCH₂CH₂CH₂—CO₂H (R) cis H — H — (phenyl)₂ phenyl 39 —CH₂CHR⁵— —CHR³— —C(O)CH—OCH₂CH═CH —CO₂H (S) cis H — H — (phenyl)₂ phenyl 40 —CH₂CHR⁵— —CHR³——C(O)CH —OCH₂CH₂CH₂ —CO₂H (S) cis H — H — (phenyl)₂ phenyl 41 ——CHR³CHR⁴CH₂— —C(O)CH —CH₂CH═CHphenyl —CO₂H (S) cis H — H — (phenyl)₂ 42— —CHR³CHR⁴CH₂— —C(O)CH —CH₂CH₂CH₂ —CO₂H (S) cis — — — — (phenyl)₂phenyl 43 —CR⁵— —CHR³CHR⁴— —C(O)CH (phenyl)₂ — — — — —CH (CO₂H)— —

44 —CHR⁵— —CHR³CHR⁴— —C(O)CH —C(O)NHCH₂phenyl —CO₂H (S) cis H — H —(phenyl)₂ 45 —CHR⁵— —CHR³CHR⁴— —C(O)CH —C(O)NHCH₂CH₂ —CO₂H (S) cis H — H— (phenyl)₂ phenyl 46 —CHR⁵— —CHR³CHR⁴— —C(O)CH —NHCH₂CH₂phenyl —CO₂H(S) cis H — H — (phenyl)₂ 47 —CHR⁵— —CHR³CHR⁴— —C(O)CH -1-(4-phenyl)—CO₂H (S) cis H — H — (phenyl)₂ piperidine 48 —CHR⁵— —CHR³CHR⁴— —C(O)CH-1-(3S-phenyl) —CO₂H (S) cis H — H — (phenyl)₂ piperidine 49 —CHR⁵——CHR³CHR⁴— —C(O)CH -1-(3R-phenyl) —CO₂H (S) cis H — H — (phenyl)₂piperidine 50 —CHR⁵— —CHR³CHR⁴— —C(O)CH -1-(3R/S-phenyl) —CO₂H (S) cis H— H — (phenyl)₂ piperidine 51 —CHR⁵— —CHR³CHR⁴— —C(O)CH -1-(3R-benzyl)—CO₂H (S) cis H — H — (phenyl)₂ piperidine 52 —CHR⁵— —CHR³CHR⁴— —C(O)CH-1-(3S-benzyl) —CO₂H (S) cis H — H — (phenyl)₂ piperidine 53 —CHR⁵——CHR³CHR⁴— —C(O)CH -1-(3R/S-benzyl) —CO₂H (S) cis H — H — (phenyl)₂piperidine 54 —CHR⁵— —CHR³CHR⁴— —C(O)CH —CH₂OCH₂phenyl —CO₂H (S) cis H —H — (phenyl)₂ 55 —CHR⁵— —CHR³CHR⁴— —C(O)CH —CH₂CH₂OCH₂ —CO₂H (S) cis H —H — (phenyl)₂ phenyl 56 —CHR⁵— —CHR³CHR⁴— —C(O)CH -2-(5-phenyl) —CO₂H(S) cis H — H — (phenyl)₂ oxazolyl 57 —CHR⁵— —CHR³CHR⁴— —C(O)CH-2-(5-benzyl) —CO₂H (S) cis H — H — (phenyl)₂ oxazolyl 58 —CHR⁵——CHR³CHR⁴— —C(O)CH —CH₂SO₂CH₂CH₂ —CO₂H (S) cis H — H — (phenyl)₂ phenyl59 —CHR⁵— —CHR³CHR⁴— —C(O)CH -1-(2S-benzyl) —CO₂H (S) cis H — H —(phenyl)₂ pyrrolidinyl 60 —CHR⁵— —CHR³CHR⁴— —C(O)CH -1-(2R-benzyl) —CO₂H(S) cis H — H — (phenyl)₂ pyrrolidinyl 61 —CHR⁵— —CHR³CHR⁴— —C(O)CH-1-(2R/S-benzyl) —CO₂H (S) cis H — H — (phenyl)₂ pyrrolidinyl 62 —CHR⁵——CHR³CHR⁴— —C(O)CH —N(CH₃)CH₂CH₂ —CO₂H (S) cis H — H — (phenyl)CH₂phenyl (cyclohexyl) 63 —CHR⁵— —CHR³CHR⁴— —C(O)CH (phenyl)₂

—CO₂H (S) cis H — H — 64 —CHR⁵— —CHR³CHR⁴— —C(O)CH —NHC(O)N(phenyl)₂—CO₂H (S) cis H — H — (phenyl)₂ 65 —CHR⁵— —CHR³CHR⁴— —C(O)CH (phenyl)₂

—CO₂H (S) cis H — H — 66 —CHR⁵— —CH₂CHR³— —C(O)CH —N(CH₃)CH₂CH₂CH₂ —CO₂H(S/R) cis — — H — (phenyl)₂ phenyl 67 —CHR⁵— —CH₂CHR³— —C(O)CH—N(CH₃)CH₂CH₂CH₂ —CO₂H (S/R) trans — — H — (phenyl)₂ phenyl 68 —CHR⁵——CHR³CHR⁴— —C(O)CH 1-(2S-benzyl) —CO₂H (S) cis H — H — (phenyl)₂piperidine 69 —CHR⁵— —CHR³CHR⁴— —C(O)CH 1-(2R-benzyl) —CO₂H (S) cis H —H — (phenyl)₂ piperidine 70 —CHR⁵— —CHR³CHR⁴— —C(O)CH 1-(2R/S-benzyl)—CO₂H (S) cis H — H — (phenyl)₂ piperidine 71 —CHR⁵— —CHR³CHR⁴— —C(O)CH—OCH₂-4-(2-phenyl) —CO₂H (S) cis H — H — (phenyl)₂ oxazolyl 72 —CHR⁵——CHR³CHR⁴— —C(O)CH (phenyl)₂

—CO₂H (S) cis H — H — 73 —CHR⁵— —CHR³CHR⁴— —C(O)CH (phenyl)₂

—CO₂H (S) cis H — H — 74 —CHR⁵— —CHR³CHR⁴— —C(O)CH (phenyl)₂

—CO₂H (S) cis H — H — 75 —CHR⁵— —CHR³CHR⁴— —C(O)CH (phenyl)₂

—CO₂H (S) cis H — H — 76 —CHR⁵— —CHR³CHR⁴— —C(O)CH —OCH₂CH₂CH₂ —CO₂H (R)cis H — H — (phenyl)₂ phenyl 77 —CH₂CHR⁵— —CHR³— —C(O)CH (phenyl)₂ ——CO₂H (R) — — —

78 —CH₂CHR⁵— —CHR³— —C(O)CH (phenyl)₂ — —CO₂H (R) — — —

79 —CHR⁵— —CHR³CHR⁴— —C(O)CH —O-4-(2-phenyl) —CO₂H (S) cis H — H —(phenyl)₂ oxazolyl 80 —CHR⁵— —CHR³CHR⁴— —C(O)N —OCH₂CH₂CH₂ —CO₂H (S) cisH — H — (phenyl)₂ phenyl 81 —CHR⁵— —CHR³CHR⁴— —C(O)CH -1-(3R-benzyl)—CO₂H (S) trans H — H — (phenyl)₂ piperidine 82 —CHR⁵— —CHR³CHR⁴——C(O)CH -1-(3R/S-benzyl) —CO₂H (S) trans H — H — (phenyl)₂ piperidine 83—CHR⁵— —CHR³CHR⁴— —C(O)CH -1-(3S-benzyl) —CO₂H (S) trans H — H —(phenyl)₂ piperidine 84 —CHR⁵— —CHR³CHR⁴— —C(O)CH (phenyl)₂

—CO₂H (S) cis H — H — 85 —CHR⁵— —CHR³CHR⁴— —C(O)CH (phenyl)₂

—CO₂H (S) cis H — H — 86 —CHR⁵— —CHR³CHR⁴— —C(O)CH -3R-phenylpyrrolidine—CO₂H (S) cis H — H — (phenyl)₂ 87 —CHR⁵— —CHR³CHR⁴— —C(O)CH-3S-phenylpyrrolidine —CO₂H (S) cis H — H — (phenyl)₂ 88 —CHR⁵——CHR³CHR⁴— —C(O)CH -4-(2S-benzyl) —CO₂H (S) cis H — H — (phenyl)₂morpholine 89 —CHR⁵— —CHR³CHR⁴— —C(O)CH -4-(2R-benzyl) —CO₂H (S) cis H —H — (phenyl)₂ morpholine 90 —CHR⁵— —CHR³CHR⁴— —C(O)CH —N(CH₃)(CH₂)₄-—CO₂H (S) cis H — H — (phenyl)₂ phenyl 91 —CHR⁵— —CHR³CHR⁴— —C(O)CH—N(CH₃)(CH₂)₃ —CO₂H (S) cis H — H — (phenyl)₂ (4-fluorophenyl) 92 —CHR⁵——CHR³CHR⁴— —C(O)CH —N(CH₃)(CH₂)₃- —CO₂H (S) cis H — H — (phenyl)₂(4-methoxy-3- methylphenyl) 93 —CHR⁵— —CHR³CHR⁴— —C(O)CH —N(CH₃)(CH₂)₃—CO₂H (S) cis H — H — (phenyl)₂ (3-pyridine) 94 —CHR⁵— —CHR³CHR⁴——C(O)CH —NHC(O)CH═CH —CO₂H (S) cis H — H — (Phenyl)₂ phenyl 95 —CHR⁵——CHR³CHR⁴— —C(O)CH —N(CH₃)C(O)CH═CH —CO₂H (S) cis H — H — (Phenyl)₂phenyl 96 —CHR⁵— —CHR³CHR⁴— —C(O)CH —NHC(O)CH₂CH₂ —CO₂H (S) cis H — H —(Phenyl)₂ phenyl 97 —CHR⁵— —CHR³CHR⁴— —C(O)CH —N(CH₃)C(O)CH₂CH₂ —CO₂H(S) cis H — H — (Phenyl)₂ phenyl 98 —CHR⁵— —CHR³CHR⁴— —C(O)CH—N(C(O)CH₃)CH₂CH₂ —CO₂H (S) cis H — H — (Phenyl)₂ CH₂phenyl 99 —CHR⁵——CHR³CHR⁴— —C(O)CH —N(SO₂CH₃)CH₂ —CO₂H (S) cis H — H — (Phenyl)₂CH₂CH₂phenyl 100 —CHR⁵— —CHR³CHR⁴— —C(O)CH -1-(5-phenyl-1,2,3- —CO₂H (S)cis H — H — (Phenyl)₂ triazolyl 101 —CHR⁵— —CHR³CHR⁴— —C(O)CH-1-(5-benzyl-1,2,3- —CO₂H (S) cis H — H — (Phenyl)₂ triazolyl) 102—CHR⁵— —CHR³CHR⁴— —C(O)CH -4-(5-benzyl-3-oxo- —CO₂H (S) cis H — H —(Phenyl)₂ morpholinyl) 103 —CHR⁵— —CHR³CHR⁴— —C(O)CH —OCH₂CH₂CH₂ —CH₂OH(S) cis H — H — (Phenyl)₂ phenyl 104 —CHR⁵— —CHR³CHR⁴— —C(O)CH—OCH₂CH₂CH₂-(4- —CO₂H (S) cis H — H — (Phenyl)₂ fluorophenyl) 105 —CHR⁵——CHR³CHR⁴— —C(O)CH —N(CH₃)CH₂C≡C- —CO₂H (S) cis H — H — (Phenyl)₂(3-methyl-4- methoxyphenyl) 106 —CHR⁵— —CHR³CHR⁴— —C(O)CH —CH₂CH₂CH₂CH₂—CO₂H (S) cis H — H — (Phenyl)₂ phenyl 107 —CHR⁵— —CHR³CHR⁴— —C(O)CH-2-(3-phenylthio- —CO₂H (S) cis H — H — (Phenyl)₂ phenyl) 108 —CHR⁵——CHR³— —C(O)CH —OCH₂CH₂CH₂ —CH₂OH (S/R) trans H — H — (Phenyl)₂ phenyl109 —CHR⁵— —CHR³— —C(O)CH —OCH₂CH₂CH₂ —CH₂OH (S/R) cis H — H — (Phenyl)₂phenyl 110 —CH₂CHR⁵— —CHR³— —C(O)CH —OCH₂CH═CH —CO₂H (S) trans H — H —(Phenyl)₂ phenyl 111 —CH₂CHR⁵— —CHR³— —C(O)CH —OCH₂CH₂CH₂ —CO₂H (S)trans H — H — (Phenyl)₂ phenyl 112 —CHR⁵— —CHR³CHR⁴— —C(O)CH —OCH₂CH₂CH₂—C(O)NHSO₂ cis H — H — (Phenyl)₂ phenyl N(CH₃)₂ (S) 113 —CHR⁵——CHR³CHR⁴— —C(O)CH —N(CH₃)CH₂CH₂CH₂ —C(O)NHSO₂ cis H — H — (Phenyl)₂phenyl N(CH₃)₂ (S) 114 —CHR⁵— —CHR³CHR⁴— —C(O)CH —N(CH₃)CH₂CH₂—C(O)NHSO₂ cis H — H — (Phenyl)₂ CH₂-(4-fluorophenyl) N(CH₃)₂ (S) 115—CHR⁵— —CHR³CHR⁴— —C(O)CH (Phenyl)₂

—CO₂H (S) cis H — H — 116 —CHR⁵— —CHR³CHR⁴— —C(O)CH —N(CH₃)CH₂C≡C- —CO₂H(S) cis H — H — (Phenyl)₂ phenyl 117 —CHR⁵— —CHR³CHR⁴— —C(O)CH—CH₂Ophenyl —CO₂H (S) cis H — H — (Phenyl)₂ 118 —CHR⁵— —CHR³CHR⁴——C(O)CH —CH₂SO₂CH₂ —CO₂H (S) cis H — H — (Phenyl)₂ phenyl 119 —CHR⁵——CHR³CHR⁴— —C(O)CH —CH₂SO₂phenyl —CO₂H (S) cis H — H — (Phenyl)₂ 120—CHR⁵— —CHR³CHR⁴— —C(O)CH —CH₂SCH₂CH₂ —CO₂H (S) cis H — H — (Phenyl)₂phenyl 121 —CHR⁵— —CHR³CHR⁴— —C(O)CH —CH₂SCH₂phenyl —CO₂H (S) cis H — H— (Phenyl)₂ 122 —CHR⁵— —CHR³CHR⁴— —C(O)CH —CH₂Sphenyl —CO₂H (S) cis H —H — (Phenyl)₂ 123 —CHR⁵— —CHR³CHR⁴— —C(O)CH -2-(4-phenyl-1,3- —CO₂H (S)cis H — H — (Phenyl)₂ thiazolyl) 124 —CHR⁵— —CHR³CHR⁴— —C(O)CH—SCH₂CH₂CH₂ —CO₂H (S) cis H — H — (Phenyl)₂ phenyl 125 —CHR⁵— —CHR³CHR⁴——C(O)CH —SO₂CH₂CH₂CH₂ —CO₂H (S) cis H — H — (Phenyl)₂ phenyl 126 —CHR⁵——CHR³CHR⁴— —C(O)CH —N(CH₃)CH₂CH₂O- —CO₂H (S) cis H — H — (Phenyl)₂(4-fluorophenyl) 127 —CHR⁵— —CHR³CHR⁴— —C(O)CH —CH₂N(CH₃)CH₂ —CO₂H (S)cis H — H — (Phenyl)₂ CH₂-(4-fluorophenyl) 128 —CHR⁵— —CHR³CHR⁴— —C(O)CH—N(CH₂CF₃)CH₂ —CO₂H (S) cis H — H — (Phenyl)₂ CH₂CH₂-(4- fluorophenyl)129 —CHR⁵— —CHR³CHR⁴— —C(O)CH —OCH₂CH₂CH₂ -tetrazolyl (S) cis H — H —(Phenyl)₂ phenyl 130 —CHR⁵— —CHR³CHR⁴— —C(O)CH —OCH₂CH₂CH₂ —CH₂NHSO₂ cisH — H — (Phenyl)₂ phenyl CH₃ (S) 131 —CHR⁵— —CHR³CHR⁴— —C(O)CH —SCH₂CH₂—CO₂H (S) cis H — H — (Phenyl)₂ phenyl 132 —CHR⁵— —CHR³CHR⁴— —C(O)CH—SO₂CH₂CH₂ —CO₂H (S) cis H — H — (Phenyl)₂ phenyl 133 —CHR⁵— —CHR³CHR⁴——C(O)CH —SCH₂CH₂CH₂- —CO₂H (S) cis H — H — (Phenyl)₂ (4-fluorophenyl)134 —CHR⁵— —CHR³CHR⁴— —C(O)CH —SO₂CH₂CH₂CH₂- —CO₂H (S) cis H — H —(Phenyl)₂ (4-fluorophenyl) 135 —CHR⁵— —CHR³CHR⁴— —C(O)CH —OCH₂CH₂CH₂—C(O)NHSO₂ cis H — H — (Phenyl)₂ phenyl CH₃ (S) 136 —CHR⁵— —CHR³CHR⁴——C(O)CH —N(CH₃)CH₂CH₂ —C(O)NH₂ (S) cis H — H — (Phenyl)₂CH₂-(4-fluorophenyl) 137 —CHR⁵— —CHR³CHR⁴— —C(O)CH —N(CH₃)CH₂CH₂ —CN (S)cis H — H — (Phenyl)₂ CH₂-(4-fluorophenyl) 138 —CHR⁵— —CHR³CHR⁴— —C(O)CH—N(CH₃)CH₂CH₂ -tetrazolyl (S) cis H — H — (Phenyl)₂ CH₂-(4-fluorophenyl)139 —CHR⁵— —CHR³CR⁴═ —C(O)CH -2-(3-phenylthio- —CO₂H (S) — H — H —(phenyl)₂ phenyl) 140 —CHR⁵— —CHR³CR⁴═ —C(O)CH —C≡CCH₂CH₂ —CO₂H (S) — H— H — (phenyl)₂ phenyl 141 —CHR⁵— —CHR³CR⁴═ —C(O)CH -2-(4-phenyl-1,3-—CO₂H (S) — H — H — (phenyl)₂ thiazolyl) 142 —CHR⁵— —CHR³— —C(O)CH—OCH₂CH₂CH₂ —CO₂H (S/R) trans H — H — (phenyl)₂ phenyl 143 —CHR⁵— —CHR³——C(O)CH —OCH₂CH₂CH₂ —CO₂H (S/R) cis H — H — (phenyl)₂ phenyl 144 —CHR⁵——CHR³CHR⁴— —C(O)CH -4-(2R-phenyl) —CO₂H (S) cis H — H — (phenyl)₂morpholine 145 —CHR⁵— —CHR³CHR⁴— —C(O)CH -4-(2S-phenyl) —CO₂H (S) cis H— H — (phenyl)₂ morpholine 146 —CHR⁵— —CHR³CHR⁴— —C(O)CH —N(CH₃)(CH₂C≡CH—CO₂H (S) cis H — H — (phenyl)₂ 147 —CHR⁵— —CHR³CHR⁴— —C(O)CH—N(CH₃)(CH₂ —CO₂H (S) cis H — H — (phenyl)₂ CH₂CH₃ 148 —CHR⁵— —CHR³CHR⁴——C(O)CH —N(CH₃)(CH₂C≡CC —CO₂H (S) cis H — H — (phenyl)₂ (CH₃)₃ 149—CHR⁵— —CHR³CHR⁴— —C(O)CH —N(CH₃)(CH₂CH₂ —CO₂H (S) cis H — H — (phenyl)₂CH₂C(CH₃)₃

Particular compounds of the formula (II) include compounds 2, 3, 5, 6,8, 9, 15, 16, 17, 21, 22, 23, 28, 34, 35, 36, 46, 48, 49, 50, 51, 53,54, 55, 56, 58, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 75, 76, 84,85, 86, 87, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103,104 105, 106, 107, 108, 109, 112, 114, 115, 116, 118, 119, 120, 121,122, 124, 125, 126, 131, 132, 133, 134, 135, 136, 137, 138, 139, 140,142 and 143, especially 2, 3, 5, 6, 9, 15, 16, 21, 22, 23, 28, 48, 49,50, 51, 53, 54, 55, 56, 58, 61, 63, 70, 84, 85, 87, 90, 91, 92, 93, 97,98, 100, 101, 102, 106, 107, 112, 114, 115, 118, 121, 122, 124, 126,135, 136, 137, 138, and 143.

In some embodiments, the compounds of formula (I) are selective AT₂receptor antagonists. In particular embodiments, the selective AT₂receptor antagonists have an IC₅₀ at the AT₂ receptor of ≦100 nM and anIC₅₀ at the AT₁ receptor of >100,000 nM (10 μM) using the assaymethodologies described in Biological Examples 1 and 2.

The compounds of the invention are made by methods known in the art fromcommercially available starting materials.

For preparation of pyrrolidine derivatives, starting materials includesuitably protected carboxylic acids such as trans-4-hydroxyproline ethylester and 4-hydroxy-indol-2-yl carboxylic acid methyl ester. Forpreparation of azetidine derivatives, a suitable starting materialincludes 3-hydroxy-azetidine-2-carboxylic acid methyl ester.

R² may be introduced by alkylation reactions such as reaction of analkyl or aryl chloride in the presence of base. In some instances, thebase used may be a hindered alkoxide such as tert-butoxide. In someinstances where epimerization of a group alpha to the carboxylic acid isa problem, silver oxide mediated alkylation may be used.

R¹ may be introduced either before the introduction of R² or after theintroduction of R². If R² is introduced prior to the introduction of R¹,it may be necessary to protect the ring nitrogen during the alkylationreaction. Suitable nitrogen protecting groups are known in the art, forexample, in Greene & Wutz, Protective Groups in Organic Synthesis, ThirdEdition, John Wiley & Sons, 1999. A suitable nitrogen protecting groupis t-butoxycarbonyl (Boc). Alternatively other reactive alkyl or arylgroups, such as phenoxy groups may be introduced by reaction of the4-hydroxy substituent with the phenolic hydroxyl group in the presenceof triphenylphosphine (PPh₃) and DBAD.

R¹ may be introduced by amide formation with a suitable carboxylic acidand the ring nitrogen. Amide formation is well known in the art and mayinvolve the activation of the carboxylic acid, for example, the carboxygroup is activated by formation of a carbodiimide, triazole or a uroniumor phosphonium salt of a non-nucleophilic anion. Suitable activatinggroups are well known in the art including dicyclohexylcarbodiimide(DCC), diisopropylcarbodiimide (DIC),1-ethyl-3-(dimethylaminopropyl)carbodiimide (EDCI),1-hydroxybenzotriazole (HOBt), 1-hydroxy-7-aza-benzotriazole (HOAt),ethyl-2-cyano-2-cyano-2-(hydroxyimino)acetate (Oxyma Pure),O-benzotriazole-N,N,N′,N′-tetramethyluronium hexafluorophosphate (HBTU),O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluroniumhexafluorophosphate (HATU),O-(6-chloro-1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluroniumtetrafluorophosphate (HCTU),O-benzotriazol-1-yl-N,N,N′N′-tetramethyluronium tetrafluoroborate(TBTU), (benzotriazol-1-yloxy)tripyrrolidinophosphoniumhexafluorophosphate (PyBOP);(benzotriazol-1-yloxy)-tris-(dimethylamino)phosphoniumhexafluorophosphate (BOP),(1-cyano-2-ethoxy-2-oxoethylidenaminooxy)-dimethylamino-morpholino-carbeniumhexafluorophosphate (COMU) andO-[(ethoxycarbonyl)-cyanomethyleneamino]-N,N,N′,N′-tetramethyluroniumtetrafluoroborate (TOTU).

Compounds in which R² is a substituted amino group may be prepared from4-aminoproline. 4-Aminoproline may be prepared from commerciallyavailable 4-hydroxyproline by reductive amination of a ketone resultingfrom the oxidation of the 4-hydroxy group. The amino group may befurther alkylated, acylated or sulfonated with one or two substituents.When the amine is bulky, for example, a secondary amine or the amino ofa heterocyclic ring, this method provides good yields. In an alternativeapproach, the hydroxyl group of the 4-hydroxyproline may be mesylatedand reacted with an amine nucleophile. This approach may be used whenthe amino nucleophile is a primary amine group. After introduction ofthe amino substituent, the amino group may be alkylated to provide atertiary amine such as a N-methylalkylphenyl substituent.

In some cases, where the bond to R² is with the nitrogen atom of aheterocyclic ring, the starting material may be 4-oxo-proline methylester or an N-protected or N-derivative thereof and the reactionproceeds at elevated temperature, such as between 100 and 110° C.

The mesylate may also be used to prepare compounds in which R² is athiol or sulfoxide group. For example the mesylate formed from4-hydroxy-proline methyl ester may be reacted with PhC(O)SH to provide aprotected thiol group as R². The thiol may be deprotected with mild basesuch as K₂CO₃. The free thiol may then be alkylated or arylated bymethods known in the art such as reaction with an alkyl halide. The thiogroup may also be oxidised to provide a sulfoxide, for example, withm-CPBA.

When the pyrrolidine ring has a double bond in the 3,4-position, thismay also be formed from reaction of 4-oxo-proline with a compound suchas PhNTf₂. The triflate formed may then be further reacted with anothergroup such as a heterocycle via its borate or an alkyne in the presenceof a catalyst such as CuI, Pd(PPh)₂Cl₂.

In some instances, R² may be formed into a heterocyclyl ring in situ bycyclization of a disubstituted amino group. For example, the4-oxo-proline may be aminated with a hydroxy containing alkyl amine,followed by acylation of the nitrogen atom with an chloroalkylacylchloride. The remaining chloride is able to be used in a cyclizationreaction in the presence of Cs₂CO₃.

Triazoles may be prepared by reaction of 4-azo-proline with an alkyne inthe presence of a suitable catalyst such as Cp*Ru (COD)Cl.

R³ may be a carboxy group or may be manipulated, for example byreduction with a reagent such as LiAlH₂Cl, NaBH₄/ClCO₂Et or BH₃ THF, togive a primary alcohol. Acyl sulfonamides may also be prepared byreaction with appropriate amines such as NH₂SO₂N(CH₃)₂.

The substituents of R² and R⁵ that have reactive functional groups suchas double bonds or triple bonds may be further manipulated to providevariation in the R² or R⁵ substituents. For example, double bonds may bereduced to alkylene groups, or may be oxidized such as withmeta-chloroperoxybenzoic acid (MCPBA) to give epoxides or reacted withdiiodomethane to provide cyclopropyl groups. Triple bonds may beselectively reduced to provide double bonds and catalysts may beselected to provide either cis or trans geometric isomers as known inthe art.

Substituents may be introduced onto a ring formed by R² and R⁵ in asimilar manner as discussed for the introduction of R² above.

Methods of the Invention

In one aspect of the present invention, there is provided a method oftreating or preventing the symptoms of a neuropathic condition in asubject comprising administering a compound of formula (I) or apharmaceutically acceptable salt thereof.

The compounds of formula (I) are effective in the prevention orattenuation of the symptoms of neuropathic conditions including primaryand secondary neuropathic conditions. In accordance with the presentinvention, the compounds of formula (I) can act to treat, prevent orattenuate one or more symptoms associated with neuropathic conditionsincluding, but not limited to, hyperesthesia, hyperalgesia, allodyniaand/or spontaneous burning pain. In some embodiments, the compound offormula (I) is used to prevent or attenuate one or more symptomsassociated with peripheral neuropathic conditions, illustrative examplesof which include numbness, weakness, burning pain, shooting pain, andloss of reflexes. The pain may be severe and disabling. In someembodiments, the symptom, which is the subject of the prevention and/orattenuation, is neuropathic pain. Accordingly, in a related aspect, theinvention provides methods for preventing and/or attenuating neuropathicpain in an individual, comprising administering to the individual apain-preventing or -attenuating effective amount of an AT₂ receptorantagonist, which is suitably in the form of a pharmaceuticalcomposition.

There are many possible causes of neuropathy and neuropathic pain and itwill be understood that the present invention contemplates the treatmentor prevention of symptoms of any neuropathic condition regardless of thecause. In some embodiments, the neuropathic conditions are a result ofdiseases of the nerves (primary neuropathy) and neuropathy that iscaused by systemic disease (secondary neuropathy) such as but notlimited to: diabetic neuropathy; Herpes Zoster (shingles)-relatedneuropathy; uremia-associated neuropathy; amyloidosis neuropathy; HIVsensory neuropathies; hereditary motor and sensory neuropathies (HMSN);hereditary sensory neuropathies (HSNs); hereditary sensory and autonomicneuropathies; hereditary neuropathies with ulcer-mutilation;nitrofurantoin neuropathy; tomaculous neuropathy; neuropathy caused bynutritional deficiency, neuropathy caused by kidney failure and complexregional pain syndrome. Other causes include repetitive activities suchas typing or working on an assembly line, medications known to causeperipheral neuropathy such as several antiretroviral drugs ddC(zalcitabine) and ddI (didanosine), antibiotics (metronidazole, anantibiotic used for Crohn's disease, isoniazid used for tuberculosis),gold compounds (used for rheumatoid arthritis), some chemotherapy drugs(such as vincristine and others) and many others. Chemical compounds arealso known to cause peripheral neuropathy including alcohol, lead,arsenic, mercury and organophosphate pesticides. Some peripheralneuropathies are associated with infectious processes (such asGuillian-Barre syndrome). In certain embodiments, the neuropathiccondition is a peripheral neuropathic condition, which is suitably painsecondary to mechanical nerve injury or painful diabetic neuropathy(PDN) or related condition.

The neuropathic condition may be acute or chronic and, in thisconnection, it will be understood by persons of skill in the art thatthe time course of a neuropathy will vary, based on its underlyingcause. With trauma, the onset of symptoms may be acute, or sudden;however, the most severe symptoms may develop over time and persist foryears. Inflammatory and some metabolic neuropathies have a subacutecourse extending over days to weeks. A chronic course over weeks tomonths usually indicates a toxic or metabolic neuropathy. A chronic,slowly progressive neuropathy over many years such as occurs withpainful diabetic neuropathy or with most hereditary neuropathies or witha condition termed chronic inflammatory demyelinatingpolyradiculoneuropathy (CIDP). Neuropathic conditions with symptoms thatrelapse and remit include the Guillian-Barre syndrome.

In another aspect of the invention there is provided a method oftreating or preventing a condition characterized by neuronalhypersensitivity in a subject comprising administering a compound offormula (I) or a pharmaceutically acceptable salt thereof.

In some embodiments, the condition characterized by neuronalhypersensitivity is a hyperalgesic condition such as fibromyalgia. Inother embodiments, the condition is irritable bowel syndrome which ischaracterized by neuronal hypersensitivity in the gut.

In another aspect of the invention there is provided a method oftreating or preventing a disorder associated with aberrant nerveregeneration comprising administering a compound of formula (I) or apharmaceutically acceptable salt thereof.

In some embodiments, the disorder associated with aberrant nerveregeneration also includes neuronal hypersensitivity. For example,disorders associated with aberrant nerve regeneration are breast pain,interstitial cystitis and vulvodynia. In other embodiments, the disorderis a cancer chemotherapy-induced neuropathy.

In another aspect of the invention, there is provided a method oftreating or preventing inflammatory pain in a subject comprisingadministering a compound of formula (I) or a pharmaceutically acceptablesalt thereof.

Pain related to inflammation may be acute or chronic and can be due to anumber of conditions that are characterized by inflammation including,without limitation, burns such as chemical, frictional or chemicalburns, autoimmune diseases such as rheumatoid arthritis andosteoarthritis, inflammatory bowel disease such as Crohn's disease andcolitis, and other inflammatory diseases such as inflammatory boweldisease, carditis, dermatitis, myositis, neuritis and collagen vasculardiseases.

In a further aspect, the present invention provides a method of treatingor preventing impaired nerve conduction velocity in a subject comprisingadministering a compound of formula (I) or a pharmaceutically acceptablesalt thereof.

Impaired neuronal conduction velocity is a symptom of nerve dysfunctionor damage and may be present as a symptom of a large number of diseasesor disorders, particularly diseases or disorders that exhibitparesthesia as a symptom. In some embodiments, the impaired nerveconduction velocity is associated with a neuropathic condition asdescribed above. In other embodiments, the impaired nerve conductionvelocity is associated with Carpel Tunnel Syndrome, ulnar neuropathy,Guillian-Barré Syndrome, fascioscapulohumeral muscular dystrophy andspinal disc herneation.

Nerve conduction velocity is assessed by evaluating the electricalconduction of motor and sensory nerves in the body. Motor nerveconduction velocity is measured by stimulation of a peripheral nerve andmeasuring the time taken for the electrical impulse to be detected inthe muscle associated with the nerve. The time taken is measured inmilliseconds and is converted to a velocity (m/s) by taking into accountthe distance travelled. Sensory nerve conduction is assessed in asimilar manner with stimulation of a peripheral nerve and recording at asensory site such as a finger or paw pad.

In yet a further aspect of the invention there is provided a method ofproducing analgesia in a subject comprising administering a compound offormula (I) or a pharmaceutically acceptable salt thereof.

In some embodiments, the subject is a subject having a neuropathiccondition, an inflammatory condition, impaired nerve conductionvelocity, a condition characterized by neuronal hypersensitivity or adisorder associated with aberrant nerve regeneration. In otherembodiments, the subject is a subject at risk of developing neuropathicpain, inflammatory pain, pain related to impaired nerve conductionvelocity, a condition characterized by neuronal hypersensitivity or adisorder associated with aberrant nerve regeneration.

In still another aspect of the invention there is provided a method oftreating or preventing a cell proliferative disorder in a subjectcomprising administering a compound of formula (I) or a pharmaceuticallyacceptable salt thereof.

In some embodiments, the cell proliferative disorder is a cancer,especially where the cancer is selected from leukaemia, melanoma,prostate cancer, breast cancer, ovarian cancer, basal cell carcinoma,squamous cell carcinoma, sarquoides, fibrosarcoma, colon cancer, lungcancer and other solid tumour cancers.

In other embodiments, the cell proliferative disorder is a non-cancerousproliferative disorder. Examples of such non-cancerous proliferativedisorders include dermatological disorders such as warts, keloids,psoriasis, proud flesh disorder and also the reduction in scar tissueand cosmetic remodelling.

In a further aspect the present invention provides a method of treatingor preventing a disorder associated with an imbalance between boneresorption and bone formation in a subject comprising administering acompound of formula (I) or a pharmaceutically acceptable salt thereof.

In some embodiments, the disorder associated with an imbalance betweenbone resorption and bone formation is osteoporosis.

The subjects, individuals or patients to be treated are mammaliansubjects including but not limited to humans, primates, livestockanimals such as sheep, cattle, pigs, horses, donkeys and goats;laboratory test animals such as mice, rats, rabbits and guinea pigs;companion animals such as cats and dogs or captive wild animals such asthose kept in zoos. In a particular embodiment, the subject is a human.

An “effective amount” means an amount necessary at least partly toattain the desired response, or to delay the onset or inhibitprogression or halt altogether, the onset or progression of a particularcondition being treated. The amount varies depending upon the health andphysical condition of the individual to be treated, the taxonomic groupof individual to be treated, the degree of protection desired, theformulation of the composition, the assessment of the medical situation,and other relevant factors. It is expected that the amount will fall ina relatively broad range that can be determined through routine trials.An effective amount in relation to a human patient, for example, may liein the range of about 0.1 ng per kg of body weight to 1 g per kg of bodyweight per dosage. The dosage is preferably in the range of 1 mg to 1 gper kg of body weight per dosage, such as is in the range of 1 mg to 1 gper kg of body weight per dosage. In one embodiment, the dosage is inthe range of 1 mg to 500 mg per kg of body weight per dosage. In anotherembodiment, the dosage is in the range of 1 mg to 250 mg per kg of bodyweight per dosage. In yet another embodiment, the dosage is in the rangeof 1 mg to 100 mg per kg of body weight per dosage, such as up to 50 mgper kg of body weight per dosage. In yet another embodiment, the dosageis in the range of 1 μg to 1 mg per kg of body weight per dosage. Dosageregimes may be adjusted to provide the optimum therapeutic response. Forexample, several divided doses may be administered daily, weekly,monthly or other suitable time intervals, or the dose may beproportionally reduced as indicated by the exigencies of the situation.

Reference herein to “treatment” and “prophylaxis” is to be considered inits broadest context. The term “treatment” does not necessarily implythat a subject is treated until total recovery. “Treatment” may alsoreduce the severity of an existing condition. The term “prophylaxis”does not necessarily mean that the subject will not eventually contracta disease condition. The term “prophylaxis” may be considered to includedelaying the onset of a particular condition. Accordingly, treatment andprophylaxis include amelioration of the symptoms of a particularcondition or preventing or otherwise reducing the risk of developing aparticular condition.

In some embodiments, the compounds of formula (I) or theirpharmaceutically acceptable salts thereof may be administered togetherwith another therapy. Administration may be in a single composition orin separate compositions simultaneously or sequentially such that bothcompounds or therapies are active at the same time in the body.

In some embodiments, the compounds of formula (I) or theirpharmaceutically acceptable salts are administered together with anothertherapy to treat neuropathic or inflammatory pain or the underlyingcondition that is causing the neuropathic or inflammatory pain oranother therapy to treat conditions characterized by neuronalsensitivity, disorders associated with aberrant nerve regeneration,proliferative disorders or disorders associated with an imbalancebetween bone resorption and bone formation. In some embodiments, theamount of the second drug may be reduced when administration is togetherwith a compound of formula (I) or a pharmaceutically acceptable saltthereof.

Suitable additional drugs to treat pain include opiates such asmorphine, codeine, dihydrocodeine, hydrocodone, acetyldihydrocodeine,oxycodone, oxymorphone and buprenorphine, and non-steroidalanti-inflammatory drugs (NSAIDs) such as aspirin, ibuprofen, naproxen,acetaminophen, diflunisal, salsalate, phenacetin, fenoprofen,ketoprofen, flurbiprofen, oxaprozin, loxoprofen, indomethacin, sulindac,etodolac, ketorolac, diclofenac, nabumetone, mefenamic acid,meclofenamic acid, flufenamic acid, tolfenamic acid, celecoxib,parecoxib, lumaricoxib, etoricoxib, firocoxib, rimesulide andlicofelone.

Examples of drugs to treat neuropathies include duloxetine, pregabalin,gabapentin, phenytoin, carbamazebine, levocarnitine, tricyclicantidepressants such as amitryptiline and sodium channel blockers suchas lidocaine.

Examples of chemotherapy drugs for proliferative disorders includecisplatin, carboplatin, camptothecin, carmustine, cyclophosphamide,dactinomycin, daunorubicin, dexamethasone, docetaxel, doxorubicin,etoposide, epirubicin, everolimus, gemcitibine, goserelin, trastuzumab(Herceptin®), idarubicin, interferon-alfa, irinotecan, methotrexate,mitomycin, oxaliplatin, paclitaxel, raloxifene, streptozocin, tamoxifen,topotecan, vinblastine, vincristine, abiraterone, fluorouracil,denosumab, imatinib, geftinib, lapatinib, pazopanib, rituximab,sunitinib, erlotinib and vorinistat.

Examples of drugs to treat disorders associated with an imbalancebetween bone formation and bone resorption include bisphosphonates suchas sodium alendronate, risedronate and ibandronate, raloxifene,calcitonin, teriparatide, strontium ranelate or calcium supplements.

Examples of drugs used to treat conditions characterized by neuronalhypersensitivity, such as irritable bowel syndrome, include 5HT₃receptor antagonists such as alosetron (Lotronex®).

The AT₂ receptor antagonists of the invention are also useful incombination with radiotherapy in cancer patients.

Compositions of the Invention

While it is possible that, for use in therapy, a compound of theinvention may be administered as a neat chemical, it is preferable topresent the active ingredient as a pharmaceutical composition.

Thus, in a further aspect of the invention, there is provided apharmaceutical composition comprising a compound of formula (I) or apharmaceutically acceptable salt thereof and at least onepharmaceutically acceptable carrier.

The carrier(s) must be “acceptable” in the sense of being compatiblewith the other ingredients of the composition and not deleterious to therecipient thereof.

Pharmaceutical formulations include those suitable for oral, rectal,nasal, topical (including buccal and sub-lingual), vaginal or parenteral(including intramuscular, sub-cutaneous and intravenous) administrationor in a form suitable for administration by inhalation or insufflation.The compounds of the invention, together with a conventional adjuvant,carrier, excipient, or diluent, may thus be placed into the form ofpharmaceutical compositions and unit dosages thereof, and in such formmay be employed as solids, such as tablets or filled capsules, orliquids such as solutions, suspensions, emulsions, elixirs, or capsulesfilled with the same, all for oral use, in the form of suppositories forrectal administration; or in the form of sterile injectable solutionsfor parenteral (including subcutaneous) use. Such pharmaceuticalcompositions and unit dosage forms thereof may comprise conventionalingredients in conventional proportions, with or without additionalactive compounds or principles, and such unit dosage forms may containany suitable effective amount of the active ingredient commensurate withthe intended daily dosage range to be employed. Formulations containingten (10) milligrams of active ingredient or, more broadly, 0.1 to twohundred (200) milligrams, per tablet, are accordingly suitablerepresentative unit dosage forms. The compounds of the present inventioncan be administered in a wide variety of oral and parenteral dosageforms. It will be obvious to those skilled in the art that the followingdosage forms may comprise, as the active component, either a compound ofthe invention or a pharmaceutically acceptable salt or derivative of thecompound of the invention.

For preparing pharmaceutical compositions from the compounds of thepresent invention, pharmaceutically acceptable carriers can be eithersolid or liquid. Solid form preparations include powders, tablets,pills, capsules, cachets, suppositories, and dispersible granules. Asolid carrier can be one or more substances which may also act asdiluents, flavouring agents, solubilizers, lubricants, suspendingagents, binders, preservatives, tablet disintegrating agents, or anencapsulating material.

In powders, the carrier is a finely divided solid which is in a mixturewith the finely divided active component.

In tablets, the active component is mixed with the carrier having thenecessary binding capacity in suitable proportions and compacted in theshape and size desired.

The powders and tablets preferably contain from five or ten to aboutseventy percent of the active compound. Suitable carriers are magnesiumcarbonate, magnesium stearate, talc, sugar, lactose, pectin, dextrin,starch, gelatin, tragacanth, methylcellulose, sodiumcarboxymethylcellulose, a low melting wax, cocoa butter, and the like.The term “preparation” is intended to include the formulation of theactive compound with encapsulating material as carrier providing acapsule in which the active component, with or without carriers, issurrounded by a carrier, which is thus in association with it.Similarly, cachets and lozenges are included. Tablets, powders,capsules, pills, cachets, and lozenges can be used as solid formssuitable for oral administration.

For preparing suppositories, a low melting wax, such as admixture offatty acid glycerides or cocoa butter, is first melted and the activecomponent is dispersed homogeneously therein, as by stirring. The moltenhomogenous mixture is then poured into convenient sized molds, allowedto cool, and thereby to solidify.

Formulations suitable for vaginal administration may be presented aspessaries, tampons, creams, gels, pastes, foams or sprays containing inaddition to the active ingredient such carriers as are known in the artto be appropriate.

Liquid form preparations include solutions, suspensions, and emulsions,for example, water or water-propylene glycol solutions. For example,parenteral injection liquid preparations can be formulated as solutionsin aqueous polyethylene glycol solution.

The compounds according to the present invention may thus be formulatedfor parenteral administration (e.g. by injection, for example bolusinjection or continuous infusion) and may be presented in unit dose formin ampoules, pre-filled syringes, small volume infusion or in multi-dosecontainers with an added preservative. The compositions may take suchforms as suspensions, solutions, or emulsions in oily or aqueousvehicles, and may contain formulatory agents such as suspending,stabilizing and/or dispersing agents. Alternatively, the activeingredient may be in powder form, obtained by aseptic isolation ofsterile solid or by lyophilization from solution, for constitution witha suitable vehicle, e.g. sterile, pyrogen-free water, before use.

Aqueous solutions suitable for oral use can be prepared by dissolvingthe active component in water and adding suitable colorants, flavours,stabilizing and thickening agents, as desired.

Aqueous suspensions suitable for oral use can be made by dispersing thefinely divided active component in water with viscous material, such asnatural or synthetic gums, resins, methylcellulose, sodiumcarboxymethylcellulose, or other well known suspending agents.

Also included are solid form preparations which are intended to beconverted, shortly before use, to liquid form preparations for oraladministration. Such liquid forms include solutions, suspensions, andemulsions. These preparations may contain, in addition to the activecomponent, colorants, flavours, stabilizers, buffers, artificial andnatural sweeteners, dispersants, thickeners, solubilizing agents, andthe like.

For topical administration to the epidermis the compounds according tothe invention may be formulated as ointments, creams or lotions, or as atransdermal patch. Ointments and creams may, for example, be formulatedwith an aqueous or oily base with the addition of suitable thickeningand/or gelling agents. Lotions may be formulated with an aqueous or oilybase and will in general also contain one or more emulsifying agents,stabilizing agents, dispersing agents, suspending agents, thickeningagents, or colouring agents.

Formulations suitable for topical administration in the mouth includelozenges comprising active agent in a flavoured base, usually sucroseand acacia or tragacanth; pastilles' comprising the active ingredient inan inert base such as gelatin and glycerin or sucrose and acacia; andmouthwashes comprising the active ingredient in a suitable liquidcarrier.

Solutions or suspensions are applied directly to the nasal cavity byconventional means, for example with a dropper, pipette or spray. Theformulations may be provided in single or multidose form. In the lattercase of a dropper or pipette, this may be achieved by the patientadministering an appropriate, predetermined volume of the solution orsuspension. In the case of a spray, this may be achieved for example bymeans of a metering atomizing spray pump. To improve nasal delivery andretention the compounds according to the invention may be encapsulatedwith cyclodextrins, or formulated with their agents expected to enhancedelivery and retention in the nasal mucosa.

Administration to the respiratory tract may also be achieved by means ofan aerosol formulation in which the active ingredient is provided in apressurised pack with a suitable propellant such as a chlorofluorocarbon(CFC) for example, dichlorodifluoromethane, trichlorofluoromethane, ordichlorotetrafluoroethane, carbon dioxide, or other suitable gas. Theaerosol may conveniently also contain a surfactant such as lecithin. Thedose of drug may be controlled by provision of a metered valve.

Alternatively the active ingredients may be provided in the form of adry powder, for example a powder mix of the compound in a suitablepowder base such as lactose, starch, starch derivatives such ashydroxypropylmethyl cellulose and polyvinylpyrrolidone (PVP).

Conveniently the powder carrier will form a gel in the nasal cavity. Thepowder composition may be presented in unit dose form for example incapsules or cartridges of, e.g., gelatin, or blister packs from whichthe powder may be administered by means of an inhaler.

In formulations intended for administration to the respiratory tract,including intranasal formulations, the compound will generally have asmall particle size for example of the order of 1 to 10 microns or less.Such a particle size may be obtained by means known in the art, forexample by micronization.

When desired, formulations adapted to give sustained release of theactive ingredient may be employed.

The pharmaceutical preparations are preferably in unit dosage forms. Insuch form, the preparation is subdivided into unit doses containingappropriate quantities of the active component. The unit dosage form canbe a packaged preparation, the package containing discrete quantities ofpreparation, such as packeted tablets, capsules, and powders in vials orampoules. Also, the unit dosage form can be a capsule, tablet, cachet,or lozenge itself, or it can be the appropriate number of any of thesein packaged form.

The invention will now be described with reference to the followingExamples which illustrate some preferred aspects of the presentinvention. However, it is to be understood that the particularity of thefollowing description of the invention is not to supersede thegenerality of the preceding description of the invention.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 is a graphical representation of the inhibition of neuriteoutgrowth in the presence Of angiotensin II 0.1 μM and known selectiveAT₂ receptor antagonist PD-126,055 at 0.003 μM, 0.01 μM, 0.03 μM, 0.1μM, 0.3 μM, 1 μM, 3 μM and 10 μM.

FIG. 2 is a graphical representation of the inhibition of neuriteoutgrowth in the presence of angiotensin II 0.1 μM and compound 6 at0.003 μM, 0.01 μM, 0.03 μM, 0.1 μM, 0.3 μM, 1 μM, 3 μM and 10 μM.

FIG. 3 is a graphical representation of the inhibition of neuriteoutgrowth in the presence of angiotensin II 0.1 μM and compound 16 at0.003 μM, 0.01 μM, 0.03 μM, 0.1 μM, 0.3 μM, 1 μM, 3 μM and 10 μM.

FIG. 4 is a graphical representation of the inhibition of neuriteoutgrowth in the presence of angiotensin II 0.1 μM and compound 29 at0.003 μM, 0.01 μM, 0.03 μM, 0.1 μM, 0.3 μM, 1 μM, 3 μM and 10 μM.

FIG. 5 is a graphical representation of the inhibition of neuriteoutgrowth in the presence of angiotensin II 0.1 μM and compound 38 at0.003 μM, 0.01 μM, 0.03 μM, 0.1 μM, 0.3 μM, 1 μM, 3 μM and 10 μM.

EXAMPLES Abbreviations

DCM dichloromethane DBAD dibenzyl azodicarboxylate RT room temperaturePE petroleum ether EA or EtOAc ethyl acetate THF tetrahydrofuran Et₂Odiethyl ether MeOH methanol Et₃N triethylamine DMAP4-dimethylaminopyridine DMSO dimethylsulfoxide Bn benzyl Bz benzoyl TLCthin layer chromatography DCE 1,2-dichloroethane DMF dimethylformamideNaH sodium hydride TFA trifluoroacetic acid EDCI1-ethyl-3-(3-dimethylaminopropyl)carbodiimide AcOH acetic acid TEAtriethylamine Boc t-butyloxycarbonyl TBAI tetrabutylammonium iodide HCHOformaldehyde MsCl mesyl chloride PCC pyridinium chlorochromate EDTAethylenediamine tetraacetic acid DIPEA diisopropylethylamine CuI copperiodide IPA isopropylamine CDI 1,1-carbonyldiimidazole LDA Lithiumdiisopropylamide HATU O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluroroborate

General Methods Used in the Synthesis Examples

LC-MS (Agilent):

-   -   1. LC: Agilent Technologies 1200 series, Binary Pump, Diode        Array Detector. Ultimate AQ-C18, 3 μm, 2.1×50 mm column. Mobile        phase: B (MeOH) and A (0.07% HCOOH aqueous solution). Flow Rate:        0.4 mL/min at 25° C. Detector: 214 nm, 254 nm. Gradient stop        time, 5 min. Timetable:

T (min) B (%) A (%) 0 10 90 0.2 10 90 1.2 95 5 2.8 95 5 3 10 90 5 10 90

-   -   2. MS: G6110A, Quadrupole LC/MS, Ion Source: ES-API, TIC: 50˜900        m/z, Fragmentor: 60, Drying gas flow: 10 L/min, Nebulizer        pressure: 35 psi, Drying gas temperature: 350° C., Vcap: 3500V.    -   3. Sample preparation: samples were dissolved in methanol at        1˜10 μg/mL, then filtered through a 0.22 μM filter membrane.        Injection volume: 1˜10 μL.

LC-MS (Waters):

-   -   1. LC: Waters 2695, Quaternary Pump, Waters 2996 Photodiode        Array Detector. Xbridge-C18, 3.5 μm, 2.1×50 mm column. Mobile        Phase: B (MeOH) and A (0.07% HCOOH aqueous solution). Flow Rate:        0.3 mL/min at 30° C. Detector: 214 nm, 254 nm. Gradient stop        time, 10 min. Timetable:

T (min) B (%) A (%) 0 10 90 2.5 75 25 5.0 95 5 7.5 95 5 7.6 10 90 10 1090

-   -   2. MS: Micromass QZ, TIC: 100˜900 m/z, Ion Source: ES,        Capillary: 3 kV, Cone: 3V, Extractor: 3V, Drying gas flow: 600        L/hr, cone: 50 L/hr, Desolvation temperature: 300° C., Source        temperature: 100° C.    -   3. Sample preparation: samples were dissolved in methanol at        1˜10 μg/mL, then filtered through a 0.22 μm filter membrane.        Injection volume: 1˜10 μL.

LC-MS (Agilent, P-2) (Positive Ion Mode) or LC-MS (Agilent, N-2)(Negative Ion Mode):

-   -   1. LC: Agilent Technologies 1200 series, Binary Pump, Diode        Array Detector. Xbridge-C18, 2.5 μm, 2.1×30 mm column. Mobile        phase: B (MeOH) and A (0.07% HCOOH aqueous solution). Flow Rate:        0.5 mL/min at 30° C. Detector: 214 nm, 254 nm. Gradient stop        time, 5 min. Timetable:

T (min) B (%) A (%) 0 80 20 0.2 80 20 0.8 5 95 2.8 5 95 3 80 20 5 80 20

-   -   4. MS: G6110A, Quadrupole LC/MS, Ion Source: ES-API, TIC: 50˜900        m/z, Fragmentor: 60, Drying gas flow: 10 L/min, Nebulizer        pressure: 35 psi, Drying gas temperature: 350° C., Vcap: 3500V.    -   5. Sample preparation: samples were dissolved in methanol at        1˜10 μg/mL, then filtered through a 0.22 μm filter membrane.        Injection volume: 1˜10 μL.

LC-MS (Agilent, P-1) (Positive Ion Mode) or LC-MS (Agilent, N-1)(Negative Ion Mode) (Low Polarity Samples):

-   -   1. LC: Agilent Technologies 1200 series, Binary Pump, Diode        Array Detector. Xbridge-C18, 2.5 μm, 2.1×30 mm column. Mobile        phase: B (MeOH) and A (0.07% HCOOH aqueous solution). Flow Rate:        0.4 mL/min at 30° C. Detector: 214 nm, 254 nm. Gradient stop        time, 6 min. Timetable:

T (min) B (%) A (%) 0 80 20 0.2 80 20 0.8 5 95 3.8 5 95 4 80 20 6 80 20

-   -   2. MS: G6110A, Quadrupole LC/MS, Ion Source: ES-API, TIC: 50˜900        m/z, Fragmentor: 60, Drying gas flow: 10 L/min, Nebulizer        pressure: 35 psi, Drying gas temperature: 350° C., Vcap: 3500V.    -   3. Sample preparation: samples were dissolved in methanol at        1˜10μg/mL, then filtered through a 0.22 μm filter membrane.        Injection volume: 1˜10 μL.

Analytical HPLC:

-   -   1. (Referred to as “Aligent”) Agilent Technologies 1200 series,        Quaternary Pump, Diode Array Detector. Ultimate AQ-C18, 5 μm,        4.6×250 mm column. Mobile Phase: B (MeOH) and A (0.07% TFA        aqueous solution). Flow Rate: 1.00 mL/min at 30° C. Detector:        214 nm, 254 nm. Gradient stop time: 20 min. Timetable:

T (min) B (%) A (%) 0 40 60 3 40 60 5 60 40 7 80 20 8 95 5 15 95 5 17 4060 20 40 60

-   -   2. Sample preparation: samples were dissolved in methanol at ˜1        mg/mL, then filtered through a 0.22 μm filter membrane.        Injection volume: 1˜10 pt.

Referred to as “July-L” or “SYN-001”

-   -   1. Agilent Technologies 1200 series, Quaternary Pump, Diode        Array Detector. Waters Nova-pak C18, 4 μm, 3.9×150 mm column.        Mobile Phase: C (MeOH) and D (0.07% TFA aqueous solution). Flow        Rate: 1.00 mL/min at 30° C. Detector: 214 nm, 254 nm. Gradient        stop time: 15 min. Timetables:

Method Name: SYN-901 (High Polarity)

T (min) C (%) D (%) 0 5 95 2 5 95 5 12 88 6 40 60 7 95 5 10 95 5 12 6040 13 5 95 15 5 95

Method Name: JULY-L (Average and Low Polarity)

T (min) C (%) D (%) 0 20 80 2 20 80 4 40 60 5 70 30 6 95 5 10 95 5 11 7020 12 20 80 15 20 80

-   -   2. Sample preparation: samples were dissolved in methanol at ˜1        mg/mL, then filtered through a 0.22 μm filter membrane.        Injection volume: 1˜10 μL.

Referred to as “ZSJ-2”

-   -   1. Agilent Technologies 1200 series, Quaternary Pump, Diode        Array Detector. Waters Nova-pak C18, 4 μm, 3.9×150 mm column.        Mobile Phase: C (MeOH) and D (0.07% TFA aqueous solution). Flow        Rate: 1.00 mL/min at 30° C. Detector: 214 nm, 254 nm. Gradient        stop time: 30 min. Timetable:

Method Name: ZSJ-2

T (min) C (%) D (%) 0 20 80 28 95 5 30 70 30

-   -   2. Sample preparation: samples were dissolved in methanol at ˜1        mg/mL, then filtered through a 0.22 μm filter membrane.        Injection volume: 1˜10 μL.

Example 1: Compound 2(2S,4S)-4-(benzyloxy)-1-(2,2-diphenylacetyl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of Compound 26

A solution of diphenylacetic acid (5.0 g, 23.6 mmol) in thionyl chloride(30 mL) was heated at reflux for 30 min. The mixture was thenconcentrated in vacuo and the residue was dissolved in ether (10 mL) andadded to a mixture of compound 2a (3.76 g, 25.9 mmol) and NaHCO₃ (5.95g, 70.8 mmol) in water (50 mL) and ether (20 mL) at 0° C. Afteraddition, the mixture was stirred at RT for 2 h, TLC (EA:PE=1:1) showedthe starting material was consumed. The product was collected byfiltration and the obtained filter cake was dissolved in EA (50 mL),washed with brine (30 mL×3), dried over Na₂SO₄, filtered andconcentrated in vacuo to give 2b as a white solid (6.5 g, 74%). LC-MS(Agilent): R_(t) 4.86 min; m/z calculated for C₂₀H₂₁NO₄ [M+H]⁺ 340.2,[M+Na]⁺ 362.1, found [M+H]⁺ 340.2, [M+Na]⁺ 362.1.

2. Procedure for the Preparation of Compound 2c

To a stirred solution of 2b (2.0 g, 5.9 mmol) and Et₃N (1.2 g, 11.8mmol) in DCM (20 mL) was added MsCl (0.81 g, 7.1 mmol) at 0° C. Afteraddition, the reaction was stirred at RT for 1 h. TLC (PE:EA=2:1) showedthe starting material was consumed. DCM (10 mL) and water (20 mL) wereadded and the DCM layer was separated, washed with brine (20 mL×3) thendried over Na₂SO₄. The solvent was removed in vacuo to give 2c as ayellow solid (2.0 g, 81%). LC-MS (Agilent): R_(t) 4.82 min; m/zcalculated for C₂₁H₂₃NO₆S [M+H]⁺ 418.1, [M+Na]⁺ 440.1, found [M+H]⁺418.0, [M+Na]⁺ 440.0.

3. Procedure for the Preparation of Compound 2d

To a stirred solution of 2c (2.0 g, 4.8 mmol) in DMSO (20 mL) was addedBzONa (1.4 g, 9.6 mmol) at RT. The mixture was then heated at 90° C.overnight. TLC (PE:EA=2:1) showed the starting material was consumed.The mixture was cooled to RT, added to EA (30 mL) and washed with coldwater (200 mL). The organic phase was washed with brine (2×20 mL), driedover Na₂SO₄, filtered and concentrated in vacuo. The residue waspurified by chromatography (PE:EA=10:1) to give 2d as an off-white solid(1.5 g, 70%). LC-MS (Agilent): R_(t) 5.25 min; m/z calculated forC₂₇H₂₅NO₅ [M+H]⁺ 444.2, [M+Na]⁺ 466.2, found [M+H]⁺ 444.1, [M+Na]⁺466.1.

4. Procedure for the Preparation of Compound 2e

To a stirred solution of 2d (8.0 g, 18.0 mmol) in MeOH (150 mL) wasadded K₂CO₃ (2.5 g, 18.0 mmol) at 0° C. and the mixture was stirred atRT for 1 h, TLC (PE:EA=2:1) showed the starting material was consumed.The mixture was poured into EA (200 ml), washed with water (300 mL) andbrine (150 mL×2), then dried over Na₂SO₄, filtered and concentrated invacuo. The residue was purified by chromatography (PE:EA=3:1) to give 2eas an off-white solid (5.6 g, 88%). LC-MS (Agilent): R_(t) 4.78 min; m/zcalculated for C₂₀H₂₁NO₄ [M+H]⁺ 340.2, [M+Na]⁺ 362.1, found [M+H]⁺340.0, [M+Na]⁺ 362.0.

5. Procedure for the Preparation of Compound 2f

To a stirred suspension of Ag₂O (409 mg, 1.77 mmol) in DCM (10 mL) wasadded 2e (500 mg, 1.47 mmol) at 0° C. BnBr (303 mg, 1.77 mmol) was addedto the reaction mixture at 0° C. After addition, the reaction wasstirred at RT overnight. TLC (PE:EA=1:1) showed the starting materialwas consumed. The mixture was filtered and the filtrate was concentratedin vacuo. The residue was purified by chromatography (PE:EA=0:1 to 5:1)to give the product as a clear oil (250 ing, 40%). LC-MS (Agilent):R_(t) 5.30 min; m/z calculated for C₂₇H₂₇NO₄ [M+H]⁺ 430.2, [M+Na]⁺452.2, found [M+H]⁺ 430.1, [M+Na]⁺ 452.1.

6. Procedure for the Preparation of Compound 2

To a stirred solution of 2f (250 mg, 0.58 mmol) in THF (7 mL) was addedan solution of LiOH.H₂O (37 mg, 0.87 mmol) in water (3 mL) at 0° C.After addition, the reaction was stirred overnight at 25° C. TLC(MeOH:DCM=1:10) showed the starting material was consumed. Water (5 mL)and Et₂O (10 mL) were added to the mixture and the organic phaseseparated. The aqueous phase was acidified with 1M HCl to pH 3-4 and thesolution was extracted with EA (2×10 mL). The organic layer was washedwith brine (3×10 mL) and the organic phase dried (Na₂SO₄) and evaporatedto give 200 mg of the crude product. 100 mg of the crude product waspurified by preparative TLC (MeOH:DCM=1:20) to give 59 mg of pure 2.LC-MS (Agilent): R_(t) 5.09 min; adz calculated for C₁₉H₂₅NO₅ [M+H]⁺416.2, [M+Na]⁺ 438.2, found [M+H]⁺ 416.2, [M+Na]⁺ 438.1. HPLC (214 and254 nm): R_(t) 13.38 min.

Example 2: Compound 3(2S,4R)-4-(benzyloxy)-1-(2,2-diphenylacetyl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of Compound 2a

To a stirred mixture of 3a (5.0 g, 38:1 mmol) in MeOH (50 mL) was addedSOCl₂ (5 mL) dropwise and the mixture was heated at reflux for 7 h, TLC(DCM:MeOH=10:1) showed the starting material was consumed. The MeOH wasremoved in vacuo to give 2a (6.0 g) as white solid, which was used forthe next step directly. LC-MS (Agilent): R_(t) 0.87 min; m/z calculatedfor C₆H₁₁NO₃[M+H]⁺ 146.1, found [M+H]⁺ 146.1.

2. Procedure for the Preparation of Compound 3b

To a stirred solution of 2a (4.0 g, 27.5 mmol) and Et₃N (3.3 g, 33.1mmol) in DCM (40 mL) was added (Boc)₂O (7.22 g, 33.1 mmol) at 0° C.under N₂ and the mixture was stirred at RT for 5 h, TLC (DCM:MeOH=20:1)showed the starting material was consumed. The reaction was quenchedwith water (30 mL), the layers were separated and the aqueous phase wasextracted with DCM (20 mL×2). The combined organic extracts were washedby brine, dried over Na₂SO₄ and concentrated in vacuo. Recrystallizationfrom hexane/DCM then gave 3b as white solid (4.2 g, 62%). LC-MS(Agilent): R_(t) 4.96 min; m/z calculated for C₁₁H₁₉NO₅ [M+Na]⁺ 268.1,[2M+Na]⁺ 513.3, found [M+Na]⁺ 268.1, [2M+Na]⁺ 513.3.

3. Procedure for the Preparation of Compound 3c

To a stirred suspension of 3b (2.5 g, 10.2 mmol), BnBr (1.5 mL, 12.2mmol) and TBAI (1.13 g, 3.06 mmol) in THF (50 mL) was added NaH (60% w/wdispersion in mineral oil, 0.45 g, 11.2 mmol) at 0° C. and the mixturewas stirred at RT overnight, TLC (PE:EA=2:1) showed that the startingmaterial was consumed. The mixture was poured into water (40 mL) andextracted with EA (30 mL×2). The combined organic extracts were washedwith brine, dried over Na₂SO₄ and concentrated in vacuo. Purification bysilica column (PE:EA=10:1 to 4:1) gave 3c as yellow oil (1.7 g, 50%).LC-MS (Agilent): R_(t) 5.35 min; m/z calculated for C₁₈H₂₅NO₅ [M+Na]⁺358.2, [2M+Na]⁺ 693.3, found [M+Na]⁺ 358.2, [2M+Na]⁺ 693.4.

4. Procedure for the Preparation of Compound 3d

To a stirred solution of 3c (800 mg, 2.38 mmol) in DCM (6 mL) was addedTFA (1.36 g, 12.0 mmol) and the mixture was stirred at RT for 2 h, thenheated at 35° C. for 3 h, TLC (DCM:MeOH=20:1) showed that the startingmaterial was consumed. Water (15 mL) and DCM (15 mL) were added and theaqueous phase was adjusted to pH 8 with NaHCO₃ (aq). The layers wereseparated and the aqueous layer was extracted with DCM (10 mL). Thecombined organic extracts were washed with brine, dried over Na₂SO₄ andthe solvent was removed in vacuo to give 3d (380 mg, 67%) as a yellowoil. LC-MS (Agilent): R_(t) 4.12 min; m/z calculated for C₁₃H₁₇NO₃[M+H]⁺236.1, found [M+H]⁺ 236.1.

5. Procedure for the Preparation of Compound 3e

To a solution of diphenylacetic acid (1.14 g, 5.3 mmol) in DCM (15 mL)at 0° C. was added two drops of DMF followed by oxalyl chloride (1.0 g,8.0 mmol) and the mixture was stirred at RT for 5 h then concentrated invacuo. The residue was dissolved in DCM (15 mL) and a mixture of 3d(1.15 g, 4.8 mmol) and Et₃N (0.73 g, 7.1 mmol) in DCM (20 mL) was addedat 0° C. The mixture was then stirred at RT overnight, TLC (PE:EA=2:1)showed that the starting material was consumed. Water (30 mL) was addedand the layers were separated. The aqueous phase was extracted with DCM(20 mL) and the combined organic extracts were washed with NaHCO₃(saturated aqueous solution), brine and dried over Na₂SO₄. The solventwas removed in vacuo and purification by silica column (PE:EA=20:1 to4:1) gave the product as a yellow oil (600 mg, 30%). LC-MS (Agilent):R_(t) 5.25 min; m/z calculated for C₂₇H₂₇NO₄ [M+H]⁺ 430.1, found [M+H]⁺430.1.

6. Procedure for the Preparation of Compound 3

To a stirred mixture of 3e (600 mg, 1.4 mmol) in THF (5 mL) and H₂O (2mL) was added LiOH (146.7 mg, 3.5 mmol) and the mixture was stirred atRT for 5 h, TLC (PE:EA=1:1) showed that the starting material wasconsumed. Most of the THF was removed in vacuo, water (10 mL) was addedand the mixture was acidified to pH 2-3 with 1 M aqueous HCl andextracted with EA (10 mL×2). The combined organic extracts were washedwith brine, dried over Na₂SO₄ and concentrated in vacuo. Purification bycolumn chromatography then prep-TLC (EA:DCM=1:1) gave 3 (90 mg, 17%) asa white solid.

LC-MS (Agilent): R_(t) 5.22 min; m/z calculated for C₂₆H₂₅NO₄ [M+H]⁺416.1, found [M+H]⁺ 416.1. HPLC (214 and 254 nm): R_(t) 13.49 min.

Example 3: Compound 5(2S,4S)-4-cinnamyloxy-1-(2,2-diphenylacetyl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of Compound 5a

To a stirred suspension of 2e (2.0 g, 5.89 mmol) and Ag₂O (1.64 g, 7.07mmol) in DCM (25 mL) at 0° C. was added cinnamyl bromide (1.4 g, 7.07mmol) at 0° C. and the mixture was stirred at RT overnight, TLC(PE:EA=1:1) showed most of the starting material was consumed. Thereaction was filtered and the filtrate was concentrated in vacuo. Theresidue was purified by chromatography (PE:EA=10:1 to 5:1) to give 5a asa colorless oil (270 mg, 10%). LC-MS (Agilent): R_(t) 5.43 min; m/zcalculated for C₂₉H₂₉NO₄ [M+H]⁺ 456.2, [M+Na]⁺ 478.2, found [M+H]⁺456.1, [M+Na]⁺ 478.1.

2. Procedure for the Preparation of Compound 5

To a stirred solution of 5a (270 mg, 0.59 mmol) in THF (7 mL) and H₂O (3mL) was added LiOH.H₂O (37 mg, 0.87 mmol) at 0° C. and the mixture wasstirred at 0° C. for 0.5 hour, TLC (MeOH:DCM=1:10) showed the startingmaterial was consumed. The mixture was concentrated in vacuo to removemost of the THF and water (10 mL) and Et₂O (10 mL) were added. Themixture was acidified with 1M HCl to pH 7 and then basified with sodiumbicarbonate to pH 10 and the phases separated. DCM (10 mL) was added tothe aqueous phase and the mixture was acidified to pH 3-4 with 1M HCland the organic layer was separated, washed with water (5 mL×1), brine(5 mL×2), dried over Na₂SO₄, filtered and concentrated in vacuo to givethe product (150 mg) as a white solid. The crude product was purified byprep-TLC to give 5 as a white solid (130 mg). LC-MS (Agilent): R_(t)5.26 min; m/z calculated for C₂₈H₂₇NO₄ [M+H]⁺ 442.2, [M+Na]⁺ 464.2,found [M+H]⁺ 442.1, [M+Na]⁺ 464.1. HPLC (214 and 254 nm): R_(t) 13.63min.

Example 4: Compound 6(2S,4S)-1-2,2-diphenylacetyl)-4-(3-phenylpropoxy)pyrrolidine carboxylicacid

To a stirred solution of 5 (120 mg, 0.27 mmol) in EA (3 mL) was added10% Pd/C (12 mg) and the mixture was stirred at RT under a H₂ atmosphere(1 atm pressure) overnight, TLC (MeOH:DCM=1:20) showed the startingmaterial was consumed. The mixture was filtered and the filtrate wasconcentrated in vacuo to give the crude product, which was purified bycolumn chromatography (DCM:EA=10:1 to 8:1) to give 6 (60 mg, 50%) as acolorless oil. LC-MS (Agilent): R_(t) 5.26 min; m/z calculated forC₂₈H₂₉NO₄ [M+H]⁺ 444.2, found 444.2. HPLC (214 and 254 nm): R_(t) 13.75min.

Example 5: Compound 8(2S,4R)-4-(cinnamyloxy)-1-(2,2-diphenylacetyl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of Compound 8a

A solution of diphenylacetic acid (5.0 g, 23.6 mmol) in thionyl chloride(30 mL) was heated at reflux for 30 min. The mixture was thenconcentrated in vacuo and the residue was dissolved in ether (10 mL) andadded to a mixture of 2a (3.76 g, 25.9 mmol) and NaHCO₃ (5.95 g, 70.8mmol) in water (50 mL) and ether (20 mL) at 0° C. After addition, themixture was stirred at RT for 2 h, TLC (EA:PE=1:1) showed the startingmaterial was consumed. The product was collected by filtration and theobtained cake was dissolved in EA (50 mL), washed with brine (30 mL×3),dried over Na₂SO₄, filtered and concentrated in vacuo to give 8a (6.5 g,74%) as a white solid. LC-MS (Agilent): R_(t) 4.86 min; m/z calculatedfor C₂₀H₂₁NO₄ [M+H]⁺ 340.2, [M+Na]⁺ 362.1, found [M+H]⁺ 340.2, [M+Na]⁺362.1.

2. Procedure for the Preparation of Compound 8b

To a solution of 8a (1.0 g, 2.9 mmol) in DCM (10 mL) was added Ag₂O (806mg, 3.48 mmol) at 0° C. and the mixture was stirred at RT for 30 min. Asolution of cinnamyl bromide (685.8 mg, 3.48 mmol) in DCM (2 mL) wasthen added and the mixture was stirred at RT overnight. The Ag₂O wasremoved by filtration and the filtrate was concentrated in vacuo.Purification by silica column (PE:EA=10:1 to 4:1) gave 8b as yellowsolid (100 mg, 8%). LC-MS (Agilent): R_(t) 5.34 min; m/z calculated forC₂₉H₂₉NO₄ [M+H]⁺ 456.1, [M+Na]⁺ 478.1, found [M+H]⁺ 456.1, [M+23]⁺478.1.

3. Procedure for the Preparation of Compound 8

To a mixture of 8b (170 mg, 0.37 mmol) in THF/H₂O (3 mL/1 mL) was addedLiOH (40 mg, 0.93 mmol) and the mixture was stirred at RT for 5 h, TLC(PE:EA=2:1) showed that the starting material was consumed. Most of theTHF was removed in vacuo, water (10 mL) and Et₂O (10 mL) were added andthe layers were separated. The aqueous phase was adjusted to pH 2-3 with1 M aqueous HCl and extracted with DCM (15 mL×2). The combined organicextracts were washed with brine, dried over Na₂SO₄ and the solvent wasremoved in vacuo. Purification by prep-TLC (DCM:MeOH=10:1) gave 8 as awhite solid (80 mg, 49%). LC-MS (Agilent): R_(t) 5.34 min; m/zcalculated for C₂₈H₂₇NO₄ [M+H]⁺ 442.1, found [M+H]⁺ 442.1. HPLC (214 and254 nm): R_(t) 13.71 min.

Example 6: Compound 9(2S,4R)-1-(2,2-diphenylacetyl)-4-(3-phenylpropoxy)pyrrolidine-2-carboxylicacid

To a solution of 8 (100 mg, 0.23 mmol) in EA (5 mL) was added 10% Pd/C(10 mg) and the mixture was stirred at RT under a hydrogen atmosphere (1atm pressure) overnight. The mixture was filtered through Celite and thefiltrate was concentrated in vacuo. Purification by prep-TLC(DCM:MeOH=10:1) gave 9 as a white solid (93 mg, 93%). LC-MS (Agilent):R_(t) 5.40 min; m/z calculated for C₂₈H₂₉NO₄ [M+H]⁺ 444.2, [M+Na]⁺466.2, found [M+H]⁺ 444.2, [M+Na]⁺ 466.2. HPLC (214 and 254 nm): Rt13.86 min.

Example 7: Compound 154-(benzyloxy)-1-(2,2-diphenylacetyl)indoline-2-carboxlic acid

1. Procedure for the Preparation of Compound 15b

To a stirred solution of 15a (200 mg, 0.68 mmol) in MeOH (10 mL) wasadded Mg pieces (65 mg, 2.7 mmol) at RT under N₂ and the mixture wasstirred overnight at RT. TLC (EA:PE=1:10) showed the starting materialwas consumed. The mixture was poured into a cold 2 M aqueous HClsolution (4 mL) and then stirred until it became a clear solution. TheMixture was basified to pH 8˜9 with a saturated aqueous NaHCO₃ solutionand then concentrated in vacuo to remove most of the MeOH. The residuewas dissolved in EA, washed with water (5 mL) and brine (5 mL×2), driedover Na₂SO₄, then filtered and concentrated in vacuo to give 15b (180mg, 94%) as an off-white solid. LC-MS (Agilent): R_(t) 4.96 min; m/zcalculated for C₁₇H₁₇NO₃ [M+H]⁺ 284.1, [M+Na]⁺ 306.1, found [M+H]⁺284.1, [M+Na]⁺ 306.1.

2. Procedure for the Preparation of Compound 15c

To a solution of 15b (180 mg, 0.64 mmol), Et₃N (129 mg, 1.28 mmol), andDMAP (8 mg, 0.06 mmol) in DCM (10 mL) was added diphenylacetyl chloride(175 mg, 0.76 mmol) at 0° C. The mixture was then warmed to RT andstirred for 5 h, TLC (DCM) showed the starting material was consumed.Iced water was added to quench the reaction, the organic layer wasseparated, washed with brine (5 mL×2), dried over Na₂SO₄, then filteredand concentrated in vacuo. The residue was purified by chromatography(PE:DCM=10:1 to 1:2) to give 15c (220 mg, 56%) as an off-white solid.LC-MS (Agilent): R_(t) 5.50 min; m/z calculated for C₃₁H₂₇NO₄ [M+H]⁺478.2, [M+Na]⁺ 500.2, found [M+H]⁺ 478.2, [M+Na]⁺ 500.2.

3. Procedure for the Preparation of Compound 15

To a solution of 15c (50 mg, 0.10 mmol) in THF (0.7 mL) was added asolution of LiOH.H₂O (7 mg, 0.16 mmol) in water (0.3 mL) at 0° C. andthe mixture was stirred at RT overnight, TLC (MeOH:DCM=1:10) showed thestarting material was consumed. The reaction was repeated on a largerbatch of ester (170 mg, 0.36 mmol) and the reaction mixtures werecombined and concentrated in vacuo to remove most of the THF. Theresidue was dissolved in EA (10 mL), acidified to pH 4-5 using 1 M HCland the organic phase washed with water (5 mL), brine (5 mL×2) and driedover Na₂SO₄. The solvent was removed in vacuo and the crude product waswashed with hexane and Et₂O to give pure 15 (150 mg, 70%) as a whitesolid. LC-MS (Agilent): R_(t) 5.52 min; m/z calculated for C₃₀H₂₅NO₄[M+H]⁺ 464.2, [M+Na]⁺ 486.2, found [M+H]⁺ 464.2, [M+Na]⁺ 486.1. HPLC(214 and 254 nm): R_(t) 14.08 min.

Example 8: Compound 17(2S,4S)-1-(2,2-diphenylacetyl)-4-(((1R,2S)-2-phenylcyclopropyl)methoxy)pyrrolidine-2-carboxylicacid and(2S,4S)-1-(2,2-diphenylacetyl)-4-(((1S,2R)-2-phenylcyclopropyl)methoxy)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of Compound 17b

To a stirred solution of 17a (2.0 g, 6.2 mmol) in DMSO (20 mL) was addedBzONa (1.8 g, 12.4 mmol) at RT and the mixture was stirred at 90° C. for6 h, TLC (PE:EA=2:1) showed the starting material was consumed. Themixture was cooled to RT. The reaction was repeated (140 g, 434 mmol)and the two reaction mixtures were combined and poured into water (10 L)and EA (2 L). The layers were separated and the aqueous phase wasextracted with EA (0.5 L). The combined organic extracts were washedwith brine (1 L×3), dried over Na₂SO₄, filtered and concentrated invacuo to give crude 17b (150 g) as an off-white solid which was used innext step directly. LC-MS (Agilent): R_(t) 3.20 min; m/z calculated forC₁₈H₂₃NO₆ [M+H-Boc]⁺ 250.1, [M+Na]⁺ 372.1, found [M+H-Boc]⁺ 250.1,[M+Na]⁺ 372.1.

2. Procedure for the Preparation of Compound 17c

To a stirred solution of 17b (1.0 g, 2.86 mmol) in MeOH (20 mL) wasadded K₂CO₃ (0.4 g, 2.86 mmol) at 0° C. and the mixture was stirred atRT for 0.5 h, TLC (PE:EA=1:1) showed the reaction was complete. Thereaction was repeated (150 g, 429 mmol) and the two reaction mixtureswere combined and filtered. The filtrate was concentrated in vacuo toremove most of the MeOH, the residue was dissolved in EA (500 mL),washed with water (250 mL), brine (250 mL×2), dried over Na₂SO₄,filtered and concentrated in vacuo. The residue was purified bychromatography (PE:EA=1:0 to 0:1) to give 17c as an off-white solid (70g, 65%). LC-MS (Agilent): R_(t) 2.97 min; m/z calculated for C₁₁H₁₉NO₅[M+H-Boc]⁺ 146.1, [M+H-t-Bu]⁺ 190.1, [M+Na]⁺, 268.1, found [M+H-Boc]⁺146.1, [M+H-t-Bu]⁺ 190.1, [M+Na]⁺, 268.1.

3. Procedure for the Preparation of Compound 17d

To a stirred solution of the 17c (3.5 g, 14.3 mmol) in DMF (35 mL) wasadded NaH (60% w/w dispersion in mineral oil, 0.63 g, 15.7 mmol) at 0°C. under a N₂ atmosphere and the mixture was stirred at RT for 1 hourthen re-cooled to 0° C. The bromide (3.1 g, 15.7 mmol) was added and themixture was warmed to RT slowly and then stirred overnight, TLC(PE:EA=1:1) showed the starting material was consumed. The mixture waspartitioned between EA (100 mL) and water (300 mL), the layers wereseparated and the aqueous layer was extracted with EA (80 mL×2). Thecombined organic layers were washed with brine, dried over Na₂SO₄ andconcentrated in vacuo and the residue was purified by chromatography(PE:EA=10:0 to 1:20) to give 17d as a colorless oil (1.0 g, 19%). LC-MS(Agilent): R_(t) 3.25 min; m/z calculated for C₂₀H₂₅NO₅ [M+H-Boc]⁺260.1, [M+Na]⁺ 382.2, found [M+H-Boc]⁺ 260.1, [M+Na]⁺ 382.1.

4. Procedure for the Preparation of Compound 17e

To a stirred solution of compound 17d (1.0 g, 3.8 mmol) in DCM (10 mL)was added. TFA (1.7 g, 15.2 mmol) at 0° C. and the mixture was stirredat 0° C. for 4 hour, TLC (PE:EA=4:1) showed the starting material wasconsumed. The mixture was concentrated in vacuo, the residue waspartitioned between DCM (30 mL) and a saturated aqueous NaHCO₃ solution(30 mL). The organic layer was separated and washed with brine, driedover Na₂SO₄ and filtered. The filtrate was treated with Et₃N (422 mg,4.17 mmol), cooled to 0° C. and diphenylacetyl chloride (867 mg, 3.8mmol) was added in portions. The mixture was stirred at 0˜5° C. for 10min, TLC (PE:EA=2:1) showed the reaction was complete. Ice-water (40 mL)was added and the DCM layer was separated, washed with brine, dried overNa₂SO₄ and concentrated in vacuo. The residue was purified bychromatography (PE:EA=50:0 to 10:1) to give 17e (300 mg, 17%). LC-MS(Agilent): R_(t) 3.04 min; m/z calculated for C₂₉H₂₇NO₄ [M+H]⁺ 454.2,found [M+H]⁺ 454.2.

5. Procedure for the Preparation of Compound 17f

To a stirred solution of 17e (150 mg, 0.33 mmol) in EA (3 mL) was addedLindlar catalyst (15 mg) and the mixture was stirred at RT under a H₂balloon overnight, LCMS showed the reaction was complete. The mixturewas filtered and the filtrate was concentrated in vacuo to give 17f as athick oil (150 mg). LC-MS (Agilent): R₁ 3.37 min; m/z calculated forC₂₉H₂₉NO₄ [M+H]⁺ 456.2, [M+Na]⁺ 478.2, found [M+H]⁺ 456.2, [M+Na]⁺478.2.

6. Procedure for the Preparation of Compound 17g

A stirred solution of compound 17f (100 mg, 0.22 mmol) in dry DCE (10mL) was cooled to −5° C. under a N₂ atmosphere. A ZnEt₂ solution (1 M inhexane, 0.44 mL, 0.44 mmol) was added followed by CH₂I₂ (235 mg, 0.88mmol) and the mixture was warmed to RT slowly and stirred overnight, TLCshowed the reaction was complete. The mixture was concentrated in vacuo,the residue was partitioned between ether (20 mL) and water (20 mL) andthe aqueous phase was acidified to pH 2-3 with a 1 M aqueous HClsolution. The layers were separated and the aqueous layer was extractedagain with ether (20 mL). The combined organic extracts were washed withbrine, dried over Na₂SO₄, filtered and concentrated in vacuo to givecrude product as the two indicated diastereoisomers (100 mg) as a yellowoil, which was used in next step directly.

7. Procedure for the Preparation of Compound 17

To a stirred solution of 17 g-A and 17 g-B (100 mg, 0.20 mmol) in THF (5mL) and was added LiOH.H₂O/H₂O (25 mg, 0.6 mmol/l mL) and the mixturewas stirred at RT overnight, TLC (PE:EA=4:1) showed the reaction wascomplete. The mixture was concentrated in vacuo to remove most of theTHF and the residue was partitioned between DCM (20 mL) and water (20mL). The aqueous layer was acidified to pH 3˜4 with a 1 M aqueous HClsolution, the layers were separated and the aqueous layer was extractedagain with DCM (20 mL). The combined organic extracts were washed withbrine, dried over Na₂SO₄, filtered and concentrated in vacuo. Theresidue was purified by flash chromatography (DCM: MeOH=50:1) to givethe product as a mixture of the indicated diastereoisomers as a whitesolid (80 mg, 77%). LC-MS (Agilent): R_(t) 3.28 min; m/z calculated forC₂₉H₂₉NO₄ [M+H]⁺ 456.2, [M+Na]⁺ 478.2, found [M+H]⁺ 456.2, [M+Na]⁺478.2. HPLC (214 and 254 nm): R_(t) 13.70 min.

Example 9: Compound 21(2S,4S)-1-(2,2-diphenylacetyl)-4-(methyl(3-phenylpropyl)amino)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of Compound 21a

A mixture of 2c (500 mg, 1.2 mmol) and 3-phenylpropylamine (487 mg, 3.6mmol) in DMSO/DMA/NMP (1:1:1, 10 mL) was heated at 110° C. overnight,TLC (DCM:MeOH=20:1) showed that most of the starting material wasconsumed. The mixture was poured into water (50 mL) and extracted withEA (20 mL×2). The combined organic extracts were washed with brine,dried over Na₂SO₄, filtered and concentrated in vacuo. Purification bysilica column gave 21a (300 mg, 55%) as a yellow oil. LC-MS (Agilent):R_(t) 2.96 min; m/z calculated for C₂₉H₃₂N₂O₃ [M+H]⁺ 457.2, found [M+H]⁺457.2.

2. Procedure for the Preparation of Compound 21b

To a solution of compound 21a (300 mg, 0.66 mmol) in CH₃CN (8 mL) wasadded 37% aqueous HCHO (160.0 mg, 1.97 mmol) and NaCNBH₃ (103.9 mg, 1.65mmol) and the mixture was stirred at RT for 3 h, TLC (DCM:MeOH=20:1)showed that the starting material was consumed. Water (20 mL) was addedand the mixture was extracted with EA (15 mL×2). The combined organicextracts were washed with brine, dried over Na₂SO₄, concentrated invacuo and the residue was purified by silica column (DCM:MeOH=100:1 to50:1) to give 21b (280 mg, 90%) as a yellow solid. LC-MS (Agilent):R_(t) 2.95 min; m/z calculated for C₃₀H₃₄N₂O₃ [M+H]⁺ 471.2, found [M+H]⁺471.3.

3. Procedure for the Preparation of Compound 21

To a stirred mixture of 21b (280 mg, 0.6 mmol) in THF/water (6 mL/2 mL)was added LiOH.H₂O (75.0 mg, 1.8 mmol) and the mixture was stirred at RTovernight, TLC showed that the starting material was consumed. Most ofthe THF was removed in vacuo and the residue was partitioned betweenwater (20 mL) and Et₂O (10 mL). The Et₂O layer was discarded, DCM (10mL) was added and the aqueous layer was acidified to pH 2-3 with a 1 Maqueous HCl solution. The organic layer was separated and the aqueouslayer was extracted again with DCM (10 mL). The combined organicextracts were washed with brine, dried over Na₂SO₄, filtered andconcentrated in vacuo to give crude 21 (180 mg). Purification byprep-HPLC gave pure 21 (60.0 mg, 22%) as a white solid. LC-MS (Agilent):R_(t) 3.14 min; m/z calculated for C₂₉H₃₂N₂O₃ [M+H]⁺ 457.2, found [M+H]⁺457.2. HPLC (214 and 254 nm): R_(t) 14.30 min.

Example 10: Compound 22(2S,4S)-1-(2,2-diphenylacetyl)-4-(methyl(phenylethylamino)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of Compound 22a

The reaction of Example 9, 2. was repeated with 46a (380.0 mg, 0.86mmol) in CH₃CN (8 mL), 37% aqueous HCHO (210 mg, 2.6 mmol) and NaCNBH₃(135.0 mg, 2.2 mmol) to give 22a (260 mg, 66%) as a yellow solid. LC-MS(Agilent): R_(t) 2.60 min; m/z calculated for C₂₉H₃₂N₂O₃ [M+H]⁺ 457.3,found [M+H]⁺ 457.3.

2. Procedure for the Preparation of Compound 22

Hydrolysis of 22a (260 mg, 0.57 mmol) as performed using the method ofExample 9, 3. using 3 equivalents of LiOH.H₂O (71.8 mg, 1.71 mmol).Purification by prep-HPLC gave 22 (160.0 mg, 64%) as a white solid.LC-MS (Agilent): R_(t) 3.09 min; m/z calculated for C₂₈H₃₀N₂O₃ [M+H]⁺443.3, found [M+H]⁺ 443.3. HPLC (214 and 254 nm): R_(t) 12.66 min.

Example 11: Compound 23(2S,4S)-1-(2,2-diphenylacetyl)-4-(4-phenylpiperazine)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of Compound 23b

A mixture of compound 23a (1.5 g, 3.5 mmol) and N-phenylpiperazine (1.75g, 10.7 mmol) in CH₃CN (10 mL) was heated at 110° C. overnight, TLC(DCM:MeOH=20:1) showed that the reaction was complete. The mixture waspoured into water (50 mL) and extracted with EA (20 mL×2). The combinedorganic extracts were washed with brine, dried over Na₂SO₄, filtered andconcentrated in vacuo to give 23b (600 mg 35%) as a yellow solid. LC-MS(Agilent): R_(t) 3.16 min; m/z calculated for C₃₀H₃₃N₃O₃ [M+H]⁺ 484.3,found [M+H]⁺ 484.3.

2. Procedure for the Preparation of Compound 23

Hydrolysis of 23b (450 mg, 0.93 mmol) was performed using the method ofExample 9, 3. using about 3 equivalents of LiOH.H₂O (117.4 mg, 2.8mmol). Recrystallization from DCM/hexane gave 23 (200 mg, 45%) as awhite solid. LC-MS (Agilent): R_(t) 3.17 min; m/z calculated forC₂₉H₃₁N₃O₃ [M+H]⁺ 470.3, found [M+H]⁺ 470.3. HPLC (214 and 254 nm): Rt14.25 mini.

Example 12: Compound 28(2S,4S)-4-((S)-3-benzylmorpholino)-1-(2,2-diphenylacetyl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of Compound 28b

To a solution of 28a (762 mg, 2.26 mmol) and (S)-3-benzylmorpholine (400mg, 2.26 mmol) in DCE (10 mL) was added AcOH (0.2 mL) and the mixturewas stirred at RT for 40 min. The mixture was cooled to 0° C.,NaBH(OAc)₃ (954 mg, 4.5 mmol) was added and stirring was continued at RTovernight, TLC (PE:EA=2:1) showed that the starting material wasconsumed. Water (20 mL) was added and the pH was adjusted to 7-8 withNa₂CO₃. The organic phase was separated and the aqueous layer wasextracted with DCM (20 mL). The combined organic extracts were washedwith brine, dried over Na₂SO₄, filtered and concentrated in vacuo.Purification by silica column (PE:EA=10:1 to 4:1) gave 28b (400 mg, 36%)as a white solid. LC-MS (Agilent): R_(t) 3.26 min; m/z calculated forC₃₁H₃₄N₂O₄ [M+H]⁺ 499.3, found [M+H]⁺ 499.3.

2. Procedure for the Preparation of Compound 28

To a mixture of compound 28b (400 mg, 0.8 mmol) in THF/water (6 mL/2 mL)was added LiOH.H₂O (101 mg, 2.4 mmol) and the mixture was stirred at RTovernight, TLC showed the starting material was consumed. Most of theTHF was removed in vacuo and the residue was partitioned between water(20 mL) and Et₂O (15 mL) and the aqueous phase was adjusted to pH 2-3with 1 M aqueous HCl solution, then to pH 8 with Na₂CO₃. The Et₂O phasewas separated and discarded, DCM (10 mL) was added and the aqueous layerwas acidified to pH 2-3 with a 1 M aqueous HCl solution. The organiclayer was separated and the aqueous layer was extracted with DCM (20mL). The combined organic extracts were washed with brine, dried overNa₂SO₄, filtered and concentrated in vacuo. Recrystallization fromDCM/hexane gave 28 (200 mg, 51%) as a white solid. LC-MS (Agilent):R_(t) 3.10 min; m/z calculated for C₃₀H₃₂N₂O₄ [M+H]⁺ 485.3, found [M+H]⁺485.3. HPLC (214 and 254 nm): R_(t) 12.08 min

Example 13: Compound 35(2S,4S)-1-(2,2-diphenylacetyl)-4-(2-phenoxyphenoxy)-pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of Compound 35b

To a stirred solution of 35a (3.00 g, 8.84 mmol), 2-phenoxyphenol (2.40g 13.3 mmol) prepared by the method described in Synthesis, (1994, 1, p28) and PPh₃ (4.6 g, 17.7 mmol) in DCM (60 mL) was added a solution ofDBAD (5.3 g, 17.7 mmol) in DCM (30 mL) slowly at 0° C. under a N₂atmosphere and the mixture was stirred at RT overnight, TLC (PE:EA=2:1)showed the starting material was consumed. The mixture was concentratedin vacuo and the residue was partially purified by chromatography(PE:EA=1:0 to 5:1) to give 35b (6.00 g) as a colorless oil, which wasused in next step directly. LC-MS (Waters): R_(t) 6.32 min; m/zcalculated for C₃₂H₂₉NO₅ [M+H]⁺ 508.2, [M+Na]⁺ 530.2, found [M+H]⁺508.1, [M+Na]⁺ 530.1.

2. Procedure for the Preparation of Compound 35

To a solution of compound 35b (6.00 g, 11.8 mmol) in THF (35 mL) wasadded a solution of LiOH.H₂O (0.74 g, 17.7 mmol) in water (15 mL) andthe mixture was stirred at RT overnight, TLC (PE:EA=2:1) showed thestarting material was consumed. Most of the THF was removed in vacuo andthe residue was dissolved in water H₂O (10 mL) and washed with Et₂O (20mL×2). EtOAc (20 mL) was added and the aqueous layer was acidified to pH3˜4 with a 1 M aqueous HCl solution. The layers were separated and theorganic layer was washed with water (20 mL), brine (20 mL×2), dried overNa₂SO₄, filtered and concentrated in vacuo. The residue was purified bychromatography (PE to PE:EA=5:1) then prep-HPLC to give 35 (120 mg, 2%)as a white solid. LC-MS (Agilent): R_(t) 3.43 min; m/z calculated forC₃₁H₂₇NO₅ [M+H]⁺ 494.2, [M+Na]⁺ 516.2, found [M+H]⁺ 494.2, [M+Na]⁺516.2. HPLC (JULY-L) (214 and 254 nm): R_(t) 8.44 min.

Example 14: Compound 36(2S,4S)-1-(2,2-diphenylacetyl)-4-((3-phenylprop-2-yn-1-yl)-oxy)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of Compound 36b

To a stirred solution of 36a (200 mg, 1.5 mmol) and PPh₃ (430 mg, 1.65mmol) in THF (4 mL) was added CBr₄ (600 mg, 1.8 mmol) at 0° C. and themixture was stirred at 0° C. for 2 h, TLC (PE:EA=1:1) showed thestarting material was consumed. The reaction was repeated (4.8 g, 36mmol) and the reaction mixtures were combined, then most of the THF wasremoved in vacuo and the residue was partitioned between EA (50 mL) andwater (30 mL). The organic layer was separated, washed with brine (30mL×2), dried over Na₂SO₄, filtered and concentrated in vacuo. Theresidue was purified by chromatography (PE) to give 36b (6.5 g, 90%) asa colorless oil.

2. Procedure for the Preparation of Compound 36d

To a stirred suspension of 36c (100 mg, 0.29 mmol) and Ag₂O (81 mg, 0.35mmol) in DCM (2 mL) was added compound 36b (67 mg, 0.35 mmol) at 0° C.and the mixture was stirred in the dark at RT overnight. The reactionwas repeated (0.9 g, 2.6 mmol) and the reaction mixtures were combined,then the mixture was filtered and the filtrate was concentrated invacuo. The residue was purified by chromatography (PE:EA=10:1 to 5:1) togive 36d (100 mg, 8%) as a colorless oil. LC-MS (Agilent): R_(t) 3.29min; m/z calculated for C₂₉H₂₇NO₄ [M+H]⁺ 454.2, [M+Na]⁺ 476.2, found[M+H]⁺ 454.2, [M+Na]⁺ 476.2.

3. Procedure for the Preparation of Compound 36

To a mixture of compound 36d (80 mg, 0.18 mmol) in THF/water (5 mL/2 mL)was added LiOH.H₂O (11 mg, 0.26 mmol) at 0° C. and the mixture wasstirred at RT overnight, TLC (MeOH:DCM=1:10) showed the startingmaterial was consumed. The mixture was concentrated in vacuo to removemost of the THF and the residue was partitioned between EA and water.The aqueous layer was acidified to pH 3˜4 with a 1 M aqueous HClsolution and the EA layer was separated, washed with water (3 mL), brine(3 mL×2), dried over Na₂SO₄, filtered and concentrated in vacuo. Theresidue was purified by chromatography (DCM:MeOH=50:1) to give 36 (50mg, 61%) as a white solid. LC-MS (Agilent): R_(t) 3.29 min; m/zcalculated for C₂₈H₂₅NO₄ [M−H]⁻ 438.2, found [M−H]⁻ 438.1. HPLC (214 and254 nm): R_(t) 13.55 min.

Example 15: Compound 46(2S,4S)-1-(2,2-diphenylacetyl)-4-(phenethylamino)-pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of Compound 46a

A mixture of 2c (1.5 g, 3.5 mmol) and phenethylamine (1.3 g, 10.8 mmol)in DMSO (10 mL) was heated at 100° C. overnight, TLC (DCM:MeOH=20:1)showed that most of the starting material was consumed. The mixture waspoured into water and extracted with EA. The combined organic extractswere washed with brine, dried over Na₂SO₄, filtered and concentrated invacuo to give 46a (500 mg, 31%) as a yellow solid. LC-MS (Agilent):R_(t) 2.92 min; m/z calculated for C₂₈H₃₀N₂O₃ [M+H]⁺ 443.2, found [M+H]⁺443.2.

2. Procedure for the Preparation of Compound 46

To a mixture of compound 46a (200 mg, 0.45 mmol) in THF/water (6 mL/2mL) was added LiOH.H₂O (56.9 mg, 1.36 mmol) and the mixture was stirredat RT for 3 h, TLC showed that the starting material was consumed. Mostof the THF was removed in vacuo and the residue was partitioned betweenwater (20 mL) and Et₂O (10 mL). The pH of the aqueous phase was adjustedto 3-4 with a 1 M aqueous HCl solution and then to pH 8 with a saturatedaqueous Na₂CO₃ solution. The layers were separated and the Et₂O layerdiscarded. DCM (10 mL) was added and the aqueous layer was acidified topH 2-3 with a 1 M aqueous HCl solution. The layers were separated andthe organic extract was washed with brine, dried over Na₂SO₄, filteredand concentrated in vacuo. Purification by prep-HPLC gave 46 (60.0 mg,31%) as a white solid. LC-MS (Agilent): R_(t) 3.10 min; m/z calculatedfor C₂₇H₂₈N₂O₃ [M+H]⁺ 429.2, found [M+H]⁺ 429.2. HPLC (214 and 254 nm):R_(t) 11.78 min.

Example 16: Compound 48(2S,4S)-1-(2,2-diphenylacetyl)-4-((S)-3-phenylpiperidine-1-yl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of Compound 48a

A mixture of 2c (450 mg, 1.08 mmol) and (S)-3-phenyl piperidine (348 mg2.16 mmol) in CH₃CN (5 mL) heated at 105° C. in a sealed tube overnight,TLC (PE:EA=1:1) showed most of the starting material was consumed. Themixture was cooled to RT, concentrated in vacuo and the residue waspurified by chromatography (PE:EA=1:0 to 2:1) to give 48a (150 mg, 28%)as a white solid. LC-MS (Agilent): R_(t) 3.40 min; m/z calculated forC₃₁H₃₄N₂O₃ [M+H]⁺ 483.3, found [M+H]⁺ 483.3.

2. Procedure for the Preparation of Compound 48

To a mixture of compound 48a (150 mg, 0.31 mmol) in THF/water (5 mL/1mL) was added LiOH.H₂O (33 mg, 0.77 mmol) and the mixture was stirred atRT overnight, TLC (PE:EA=1:1) showed the starting material was consumed.Most of the THF was removed in vacuo and the residue was dissolved inwater (15 mL), acidified to pH 3˜4 with a 1 M aqueous HCl solution andextracted with chloroform (15 mL×2). The combined organic extracts werewashed with brine (15 mL), dried over Na₂SO₄, filtered and concentratedin vacuo to give 48 (130 mg, 89%) as a white solid. LC-MS (Agilent):R_(t) 3.55 min; m/z calculated for C₃₀H₃₂N₂O₃ [M+H]⁺ 469.2, found [M+H]⁺469.3. HPLC (JULY-L) (214 and 254 nm): R_(t) 8.87 min.

Example 17: Compound 49(2S,4S)-1-(2,2-diphenylacetyl)-4-((R)-3-phenylpiperidin-1-yl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of Compound 49a

A mixture of 2c (450 mg, 1.08 mmol) and (R)-3-phenyl piperidine (348 mg2.16 mmol) in CH₃CN (5 mL) was heated at 105° C. in a sealed tubeovernight, TLC (PE:EA=1:1) showed most of the starting material wasconsumed. The mixture was cooled to RT, concentrated in vacuo and theresidue was purified by chromatography (PE:EA=1:0 to 2:1) to give 49a(170 mg, 31%) as a colorless oil. LC-MS (Agilent): R_(t) 3.42 min; m/zcalculated for C₃₁H₃₄N₂O₃ [M+H]⁺ 483.3, found [M+H]⁺ 483.3.

2. Procedure for the Preparation of Compound 49

Hydrolysis of 49a (170 mg, 0.35 mmol) as performed with about 2equivalents of LiOH.H₂O (37 mg, 0.77 mmol) as described in Example 16,2. The resulting precipitate was collected by filtration, washed withwater (5 mL×2), then ether (5 mL×2) and dried at 45° C. overnight togive 49 (90 mg, 55%) as a white solid. LC-MS (Agilent): R_(t) 3.40 min;m/z calculated for C₃₀H₃₂N₂O₃ [M+H]⁺ 469.2, found [M+H]⁺ 469.3. HPLC(JULY-L) (214 and 254 nm): R_(t) 8.61 min.

Example 18: Compound 53(2S,4S)-4-(3-benzylpiperidin-1-yl)-1-(2,2-diphenylacetyl)-pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of Compound 53a

A mixture of 3-benzyl pyridine (1.0 g, 5.9 mmol) and PtO₂ (100 mg, 0.36mmol) in AcOH (20 mL) was stirred at 30° C. under a H₂ atmosphere (0.6Mpa) overnight, TLC (PE:EA=4:1) showed the starting material wasconsumed. The mixture was filtered and the filtrate was concentrated invacuo. The residue was partitioned between EA (30 mL) and a saturatedaqueous Na₂CO₃ solution (30 mL), the organic layer was separated, washedwith brine, dried over Na₂SO₄, filtered and concentrated in vacuo togive 53a (1.0 g, 97%) as a yellow oil. LC-MS (Waters): R_(t) 2.79 min;m/z calculated for C₁₂H₁₇N [M+H]⁺ 176.1, found [M+H]⁺ 176.2.

2. Procedure for the Preparation of Compound 53b

A mixture of compound 2c (1.2 g, 2.88 mmol) and 3-benzyl piperidine(compound 53a) (1.0 g 5.76 mmol) in CH₃CN (40 mL) was heated at 110° C.in a sealed tube overnight, TLC (PE:EA=1:1) showed the starting materialwas consumed. The mixture was cooled to RT, diluted with water andextracted with EA. The combined organic extracts were washed with brine(20 mL×2), dried over Na₂SO₄, filtered and concentrated in vacuo. Thereaction was repeated (600 mg, 1.43 mmol) and the two crude productswere combined and purified by chromatography (PE:EA=1:0 to 1:1) to give53b as the indicated mixture of diastereoisomers (300 mg, 14%) as ayellow oil. LC-MS (Waters): R_(t) 5.03 min; m/z calculated forC₃₂H₃₆N₂O₃ [M+H]⁺ 497.3, found [M+H]⁺ 497.1.

3. Procedure for the Preparation of Compound 53

To a mixture of 53b (300 mg, 0.60 mmol) in THF/water (6 mL/2 mL) wasadded LiOH.H₂O (25.4 mg, 1.8 mmol) and the mixture was stirred at RTovernight, TLC (PE:EA=1:1) showed the starting material was consumed.Most of the THF was removed in vacuo and the residue was partitionedbetween EA and water. The aqueous layer was acidified to pH 2-3 with a 1M aqueous HCl solution. The organic layer was separated, washed withwater (10 mL), brine (10 mL×2), dried over Na₂SO₄, filtered andconcentrated in vacuo. The residue was suspended in EA then heated atreflux for 30 min, cooled, the solid filtered and dried to give 53 asthe indicated mixture of diastereoisomers (80 mg, 27%) as a white solid.LC-MS (Agilent): R_(t) 3.26 min; m/z calculated for C₃₁H₃₄N₂O₃ [M+H]⁺483.3, found [M+H]⁺ 483.2. HPLC (JULY-L) (214 and 254 nm): R_(t) 7.51min

Each enantiomer of 3-benzylpiperidine was prepared using methodologydescribed in L. Micouin et al, Tetrahedron Letters, 1994, 35 (16), p.2529-2532. Compounds 51 and 52 were prepared using the respective singleenantiomer of 3-benzylpiperidine as starting material and applying thesame methodology as for the preparation of Compound 53.

Example 19: Compound 61(3′5,5′S)-2-benzyl-1′-(2,2-diphenylacetyl)-[1,3′-bipyrrolidine]-5′-carboxylicacid

1. Procedure for the Preparation of 2-Benzyl Pyrrolidine.

Racemic 2-benzyl pyrrolidine was synthesized using a modified literatureprocedure (the Sparteine chiral ligand was omitted), see: J. Am. Chem.Soc. 1994, 116, 3231 as follows:

A) Procedure for the Preparation of Boc-Protected Pyrrolidine

To a stirred mixture of pyrrolidine (10.0 g, 0.14 mol) in DCM (150 mL)at 0° C. was added TEA (15.6 g, 0.15 mol) followed by (Boc)₂O (30.6 g,0.14 mol) and the mixture was stirred at RT for 1 h, TLC showed thatpyrrolidine had disappeared. The mixture was washed with a 1 M aqueousHCl solution (100 mL), brine, dried over Na₂SO₄, filtered andconcentrated in vacuo to give the product (24.0 g, 100%) as a colorlessoil, which was used in the next step directly.

B) Procedure for the Preparation of Boc-Protected 2-Benzyl Pyrrolidine.

To a stirred solution of Boc-protected pyrrolidine (14.0 g, 80.0 mmol)in THF (200 mL) at −60° C. under N₂ was added s-BuLi (1.3 M solution inhexanes, 67.8 mL, 88 mmol) and the mixture was stirred at −60° C. for 1h. A solution of BnBr (15.4 g, 0.09 mol) in THF (5 mL) was then added at−60° C. and stirring was continued at −60° C. for a further 3 h then atRT overnight. The reaction was quenched at 0° C. with a saturatedaqueous NH₄Cl solution and extracted with EA. The organic extract waswashed with brine, dried over Na₂SO₄, filtered and concentrated invacuo. Purification by silica column (PE:EA=50:1 to 20:1) gave theproduct (6.0 g, 30%) as a yellow oil. LC-MS (Agilent): R_(t) 3.55 min;m/z calculated for C₁₆H₂₃NO₂ [M−56+H]⁺ 206.1, [M+H]⁺ 262.2, [M+Na]⁺284.1, found [M−56+H]⁺ 206.1, [M+Na]⁺ 284.1.

C) Procedure for the Preparation of Benzyl Pyrrolidine

A mixture of Boc-protected 2-benzyl pyrrolidine (6.0 g, 23.0 mmol) in a4 M HCl/ethanol solution (30 mL) was stirred at RT for 6 h, TLC(PE:EA=10:1) showed that most of the starting material had disappeared.The solvent was removed in vacuo, water (30 mL) and Et₂O (20 mL) wereadded and the layers were separated. The aqueous phase was basified topH 7-8 with a saturated aqueous Na₂CO₃ solution and extracted with DCM(2×20 mL) and CHCl₃/IPA=3:1 (v/v) (2×20 mL). The combined organicextracts were dried over Na₂SO₄, filtered and concentrated in vacuo togive the product (2.0 g, 54%) as a colorless oil. LC-MS (Agilent): R_(t)2.82 min; m/z calculated for C₁₁H₁₃N [M+H]⁺ 162.1, found [M+H]⁺ 162.1.

2. Procedure for the Preparation of Compound 61b

To a solution of compound 61a (1.0 g, 2.96 mmol) and 2-benzylpyrrolidine (0.47 g, 2.96 mmol) in DCE (20 mL) was added AcOH (0.2 mL)and the mixture was stirred at RT for 1 h. NaBH(OAc)₃ (0.94 g, 4.44mmol) was then added at 0° C. and the mixture was stirred at RTovernight, TLC (PE:EA=1:1) showed that the starting material wasconsumed. Water (20 mL) was added, the layers were separated and theaqueous layer was extracted with DCM. The combined organic layers werewashed with brine, dried over Na₂SO₄, filtered and concentrated invacuo. Purification by silica column (PE:EA=10:1 to 3:1) gave 61b as theindicated mixture of diastereoisomers (320 mg, 23%) as a white solid.LC-MS (Agilent): R_(t) 3.17 min; m/z calculated for C₃₁H₃₄N₂O₃ [M+H]⁺483.2, found [M+H]⁺ 483.2.

3. Procedure for the Preparation of Compound 61

Hydrolysis of 61b (300 mg, 0.62 mmol) as performed as described inExample 9, 3. with about 3 equivalents of LiOH.H₂O (78.4 mg, 1.87 mmol),to give 61 (200 mg, 69%) as a yellow solid. The two diastereoisomerswere separated by prep-HPLC to give compound 61-A (35 mg) and compound61-B (35 mg) as white solids. The absolute stereochemistry of thesediastereoisomers was not determined and therefore are referred to as61-A and 61-B.

Data for Compound 61-A:

LC-MS (Agilent): R_(t) 3.44 min; m/z calculated for C₃₀H₃₂N₂O₃ [M+H]⁺469.2, found [M+H]⁺ 469.2. HPLC (JULY-L) (214 and 254 nm): R_(t) 7.39min.

Data for Compound 61-B:

LC-MS (Agilent): R_(t) 3.45 min; m/z calculated for C₃₀H₃₂N₂O₃ [M+H]⁺469.2, found [M+H]⁺ 469.2. HPLC (JULY-L) (214 and 254 nm): R_(t) 7.61min.

Example 20: Compound 62(2S,4S)-1-(2-cyclohexyl-2-phenylacetyl)-4-(methyl(3-phenylpropyl)amino)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of Compound 62b

To a stirred solution of 62a (3.0 g, 12.2 mmol) and Et₃N (1.35 g, 13.4mmol) in DCM (30 mL) at 0° C. was added MsCl (1.47 g, 12.8 mmol) and themixture was stirred at 0° C. for 2 h, TLC (PE:EA=1:1) showed thestarting material was consumed. The mixture was washed with water (20mL×2), brine (20 mL), dried over Na₂SO₄, filtered and concentrated invacuo to give 62b (3.9 g, 100%) as a yellow thick oil, which was useddirectly in next step.

2. Procedure for the Preparation of Compound 62c

A solution of 62b (500 mg, 1.54 mmol) and 3-phenylpropylamine (522 mg,3.86 mmol) in CH₃CN (5 mL) was heated at 110° C. in a sealed tubeovernight and then allowed to cool to RT. The reaction was repeated(1.00 g, 3.08 mmol) and the reaction mixtures were combined andconcentrated in vacuo. The residue was dissolved in EA, washed withbrine then dried over. Na₂SO₄, filtered and concentrated in vacuo.Purification by chromatography (PE:EA=10:1 to 2:1) gave 62c (450 mg,28%) as a yellow oil. LC-MS (Agilent): R_(t) 3.11 min; m/z calculatedfor C₂₀H₃₀N₂O₄ [M+H]⁺ 363.2, found [M+H]⁺ 363.2.

3. Procedure for the Preparation of Compound 62d

To a stirred solution of 62c (450 mg, 1.24 mmol) in MeCN (10 mL) wasadded a 37% aqueous solution of formaldehyde (252 mg, 3.10 mmol)followed by AcOH (2 drops) and the mixture′ was stirred at RT for 1 h.NaCNBH₃ (195 mg, 3.10 mmol) was added and the mixture was stirred at RTovernight, TLC (DCM:MeOH=10:1) showed the starting material wasconsumed. The mixture was partitioned between EA (30 mL) and water (20mL), the organic layer was collected and washed with brine, dried overNa₂SO₄, filtered and concentrated in vacuo. The residue was purified bychromatography (PE:EA=10:1 to 2:1) to give 62d (90 mg, 19%) as a yellowoil. LC-MS (Agilent): R_(t) 2.88 min; m/z calculated for C₂₁H₃₂N₂O₄[M+H]⁺ 377.2, found [M+H]⁺ 377.2.

4. Procedure for the Preparation of Compound 62e

A suspension of compound 62d (90 mg, 0.24 mmol) in 4 M HCl/EtOH (10 mL)was stirred at RT for 4 h, TLC (DCM:MeOH=10:1) showed the startingmaterial was consumed. The mixture was concentrated in vacuo, theresidue was dissolved in water (10 mL) and washed with ether (10 mL×2).The aqueous layer was then basified to pH 9-10 with K₂CO₃ and extractedwith DCM (10 mL×2). The combined organic extracts were dried over Na₂SO₄and concentrated in vacuo. The residue was dissolved in DCM (10 mL) andcyclohexylphenyl acetic acid (50.4 mg, 0.23 mmol) and EDCI.HCl (76.6 mg,0.40 mmol) were added followed by a catalytic amount of DMAP. Themixture was then stirred at RT overnight, TLC (DCM:MeOH=20:1) showed thereaction was complete. The mixture was washed with a saturated aqueousNaHCO₃ solution (10 mL×2), brine, dried over Na₂SO₄, filtered andconcentrated in vacuo. Purification by chromatography (DCM:MeOH=1:0 to20:1) gave 62e (60 mg, 52%) as a white solid. LC-MS (Agilent): R_(t)3.24 min; m/z calculated for C₃₀H₄₀N₂O₃ [M+H]⁺ 477.3 found [M+H]⁺ 477.3.

5. Procedure for the Preparation of Compound 62

Hydrolysis of 62e (60 mg, 0.16 mmol) was performed as described inExample 2, 6. with 3 equivalents of LiOH.H₂O (15.8 mg, 0.48 mmol). Afteracidification, the organic layer was collected and washed with brine,dried over Na₂SO₄ and concentrated in vacuo to give 62 (36 mg, 49%) as awhite solid. LC-MS (Agilent): R_(t) 3.43 min; m/z calculated forC₂₉H₂₈N₂O₃ [M+H]⁺ 463.3, found [M+H]⁺ 463.3. HPLC (JULY-L) (214 and 254nm): R_(t) 7.96 min.

Example 21: Compound 63(2S,4S)-1-(2,2-diphenylacetyl)-4-(methyl((2-phenylcyclopropyl)methyl)amino)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of Compound 63f

To a stirred solution of racemic trans-2-phenyl-1-cyclopropanecarboxylicacid (2.00 g, 12.3 mmol) in dry THF (20 mL) at 0° C. was added BH₃.THF(1 M solution in THF, 14.8 mL, 14.8 mmol) and the mixture was allowed towarm slowly to RT and stirred for 4 h. More BH₃.THF (1 M solution inTHF, 7.4 mL, 7.4 mmol) was added and stirring was continued at RT for 2h, TLC (DCM:MeOH=20:1) showed the reaction was complete. The reactionwas quenched with MeOH, water was added and the mixture was extractedwith EA. The organic layer was separated and washed with brine (30mL×2), dried over Na₂SO₄, filtered and concentrated to give 63f (1.6 g,88%) as a yellow oil. LC-MS (Agilent): R_(t) 3.27 min; m/z calculatedfor C₁₀H₁₂O [M+Na]⁺ 171.1, found [M+Na]⁺ 171.1.

2. Procedure for the Preparation of Compound 63g

To a solution of 63f (0.8 g, 5.39 mmol) in THF (30 mL) was added Celite(˜3 g) followed by PCC (3.49 g, 16.2 mmol) and the mixture was stirredat RT overnight, TLC (PE:EtOAc=4:1) showed the reaction was complete.The mixture was then filtered through a plug of silica gel and rinsedwith DCM. The filtrate was concentrated in vacuo to give the product(0.62 g, 78%) as a yellow oil.

3. Procedure for the Preparation of Compound 63b

To a solution of compound 63a (1.4 g, 3.35 mmol) in DMSO (15 mL) wasadded NaN₃ (0.43 g, 6.70 mmol) and the mixture was heated at 90° C.overnight, TLC (PE:EA=2:1) showed the reaction was complete. Thereaction was partitioned between EA (30 mL) and water (60 mL), thelayers was separated and the aqueous layer was extracted with EA (20mL×2). The combined organic extracts were washed with brine (30 mL×2),dried over Na₂SO₄, filtered and concentrated to a volume of 2 mL. Amixture of THF/H₂O (10 mL/1 mL) was added followed by PPh₃ (1.4 g, 5.35mmol) and the mixture was heated at reflux for 3 h, TLC (PE:EA=2:1)showed the starting material was consumed. The mixture was concentratedin vacuo to remove most of the THF and the residue was dissolved in a0.5 M aqueous HCl solution (20 mL) and washed with EA (20 mL×2). Theaqueous layer was then basified to pH 8 with K₂CO₃ and extracted withDCM (20 mL×4). The combined organic extracts were washed with brine,dried over Na₂SO₄ and concentrated in vacuo to give 63b (1.0 g, 90%) asa white solid. LC-MS (Agilent): R_(t) 3.02 min; m/z calculated forC₂₀H₂₂N₂O₃ [M+H]⁺ 339.2, found [M+H]⁺ 339.2.

4. Procedure for the Preparation of Compound 63c

To solution of compound 63b (600 mg, 1.77 mmol) and compound 63g (260mg, 1.77 mmol) in DCE (30 mL) was added 2 drops of AcOH and the mixturewas stirred at RT for 1 h. NaBH(OAc)₃ (451 mg, 2.13 mmol) was then addedand stirring was continued at RT overnight, TLC (PE:EA=1:2) showed mostof the starting material was consumed. The mixture was washed withbrine, dried over Na₂SO₄, filtered and concentrated in vacuo. Theresidue was purified by chromatography to give 63c as a mixture of theindicated diastereoisomers (500 mg, 60%) as a yellow oil. LC-MS(Agilent): R_(t) 3.22 min; m/z calculated for C₂₀H₃₂N₂O₃ [M+H]⁺ 469.2,found [M+H]⁺ 469.2.

5. Procedure for the Preparation of Compound 63d

To a solution of compound 63c (500 mg, 1.06 mmol) in MeCN (10 mL) wasadded a 37% aqueous formaldehyde solution (220 mg, 2.66 mmol) followedby 2 drops of AcOH and the mixture was stirred at RT for 1 h. NaCNBH₃(168 mg, 2.66 mmol) was then added and stirring was continued at RTovernight, TLC (PE:EA=1:2) showed the starting material was consumed. Tothe reaction mixture was added 3-5 drops of NaHCO₃ to neutralize themixture which was partitioned between EA and water. The organic layerwas separated and washed with brine, dried over Na₂SO₄, filtered andconcentrated in vacuo. The residue was purified by chromatography(PE:EA=10:1 to 2:1) to give 63d as a mixture of the indicateddiastereoisomers (185 mg, 36%) as a yellow oil. LC-MS (Agilent): R_(t)148 min; m/z calculated for C₃₁H₃₄N₂O₃ [M+H]⁺ 483.3, found [M+H]⁺ 483.2.

6. Procedure for the Preparation of Compound 63

Hydrolysis of 63d (185 mg, 0.38 mmol) as performed as described inExample 16, 2. ith about 2.8 equivalents of LiOH.H₂O and the resultingprecipitate was collected by filtration, washed with water (5 mL×2),then purified by prep-HPLC to give 63 as a mixture of the indicateddiastereoisomers (51 mg, 28%) as a white solid. LC-MS (Agilent): R_(t)3.50 min; m/z calculated for C₃₀H₃₂N₂O₃ [M+H]⁺ 469.2, found [M+H]⁺469.3. HPLC (JULY-L) (214 and 254 nm): R_(t) 8.76 min.

Example 22: Compound 64(2S,4S)-1-(2,2-diphenylacetyl)-4-(3,3-diphenyluriedo)-pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of Compound 64b

To a stirred solution of compound 64a (300 mg, 0.88 mmol) and Et₃N (96mg, 0.96 mmol) in DCM (5 mL) was added diphenylcarbamoyl chloride (246mg, 0.96 mmol) followed a catalytic amount of DMAP and the mixture wasstirred at RT overnight, TLC (DCM:MeOH=10:1) showed the startingmaterial was consumed. Water (10 mL) was added, the layers wereseparated and the aqueous layer was extracted with DCM (10 mL). Thecombined organic extracts were washed with brine (10 mL), dried overNa₂SO₄, filtered and concentrated in vacuo. The residue was purified bychromatography (PE:EA=4:1 to 2:1) to give 64b (210 mg, 44%) as a whitesolid. LC-MS (Agilent): R_(t) 3.50 min; m/z calculated for C₃₁H₃₃N₃O₄[M+H]⁺ 534.2, [M+Na]⁺ 556.2, found [M+H]⁺ 534.2, [M+Na]+ 556.2.

2. Procedure for the Preparation of Compound 64

To a mixture of compound 64b (200 mg, 0.37 mmol) in THF (5 mL) and H₂O(1 mL) was added LiOH.H₂O (40 mg, 0.94 mmol) and the mixture was stirredat RT overnight, TLC (PE:EA=1:1) showed the starting material wasconsumed. Most of the THF was removed in vacuo and the residue wasdissolved in water (20 mL), cooled to 0° C. and acidified to pH 2-3 witha 3 M aqueous HCl solution. The resulting precipitate was collected byfiltration, washed with water (10 mL×2) and dried at 50° C. overnight togive 64 (140 mg, 72%) as a white solid. LC-MS (Agilent): R_(t) 3.52 min;m/z calculated for C₃₂H₂₉N₃O₄ [M+H]⁺ 520.2, [M+Na]⁺ 542.2, found [M+H]⁺520.2, [M+Na]⁺ 542.2. HPLC (JULY-L) (214 and 254 nm): R_(t) 8.15 min.

Example 23: Compound 65(2S,4S)-1-(2,2-diphenylacetyl)-4-(3-oxo-4-phenyl-2,8-diazaspiro[4,5]decan-8-yl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of Compound 65a

To a stirred solution of compound 3b (5.0 g, 20.4 mmol) in DCM (60 mL)was added Celite (8 g) then PCC (13.2 g, 61.2 mmol) and the mixture wasstirred at RT overnight, TLC (PE:EA=2:1) showed the starting materialwas consumed. The mixture was filtered and the filtrate was concentratedin vacuo. The residue was purified by chromatography (PE:EA=1:0 to 4:1)to give 65a (3.6 g, 72%) as a thick yellow oil. LC-MS (Agilent): R_(t)3.17 min; m/z calculated for C₁₁H₁₇NO₅ [M+H-Boc]⁺ 144.1, [M+H-t-Bu]⁺188.1, found [M+H-Boc]⁺ 144.1, [M+H-t-Bu]⁺ 188.1.

2. Procedure for the Preparation of Compound 65b

A solution of compound 65a (900 mg, 3.70 mmol) and the racemicpiperidine 65c (710 mg, 3.08 mmol) in MeOH (15 mL) was stirred at RT for30 min. NaCNBH₃ (233 mg, 3.70 mmol) was added followed by 3 drops ofAcOH and stirring was continued at RT overnight, TLC (DCM:MeOH=10:1)showed the starting material was consumed. The mixture was concentratedin vacuo and the residue was partitioned between DCM (20 mL) and asaturated aqueous NaHCO₃ solution (10 mL). The organic layer wascollected, dried over Na₂SO₄, filtered and concentrated in vacuo. Theresidue was purified by chromatography (DCM:MeOH=1:0 to 50:1) to give65b* as the indicated mixture of diastereoisomers (450 mg, 26%) as awhite solid. LC-MS (Agilent): R_(t) 3.13 min; m/z calculated forC₂₅H₃₅N₃O₅ [M+H]⁺ 458.3, found [M+H]⁺ 458.3.

3. Procedure for the Preparation of Compound 65d

To a mixture of 65b (450 mg, 0.98 mmol) in THF (10 mL) and H₂O (2 mL)was added LiOH.H₂O (104 mg, 2.46 mmol) and the mixture was stirred at RTovernight, TLC (DCM:MeOH=10:1) showed the starting material wasconsumed. Most of the THF was removed in vacuo and the residue wasdissolved in water (15 mL), cooled to 0° C., acidified to pH 2-3 with a3 M aqueous HCl solution and then freeze-dried. Purification by flashchromatography (DCM:MeOH=10:1) gave 65d as the indicated mixture ofdiastereoisomers (320 mg, 73%) as a white solid. LC-MS (Agilent): R_(t)3.20 min; m/z calculated for C₂₋₄H₃₃N₃O₅ [M+H]⁺ 444.2, found [M+H]⁺444.2. HPLC (JULY-L) (214 and 254 nm): R_(t) 8.08 min.

4. Procedure for the Preparation of Compound 65e

To a stirred suspension of 65d (270 mg, 0.61 mmol) in a 4 M HCl/dioxanesolution (5 mL) was added a 6 M aqueous HCl solution (0.5 mL). Theresulting homogeneous mixture was then stirred at RT for 2 h, LCMSanalysis showed the reaction was complete. The mixture was concentratedin vacuo to give crude 65e (250 mg) and a portion (80 mg) was purifiedby prep-HPLC to give pure 65e as the indicated mixture ofdiastereoisomers (40 mg, 59%) as a white solid. The remaining crudeproduct was used directly in the next step. LC-MS (Agilent): R_(t) 0.97min; m/z calculated for C₁₉H₂₅N₃O₃ [M+H]⁺ 344.2, found [M+H]⁺ 344.2.HPLC (JULY-L) (214 and 254 nm): R_(t) 3.19 min.

5. Procedure for the Preparation of Compound 65

To a stirred mixture of crude 65e (130 mg, 0.34 mmol) and Et₃N (86 mg,0.85 mmol) in DCM (10 mL) at 0° C. was added diphenylacetyl chloride (94mg, 0.41 mmol) in DCM (2 mL) under a N₂ atmosphere and the mixture wasstirred at 0° C. for 1 h, TLC (DCM:MeOH=10:1) showed a new product wasformed. The mixture was partitioned between DCM/water (10 mL/15 mL) andthe aqueous layer was acidified to pH 3 with a 6 M aqueous HCl solution.The organic layer was collected, concentrated in vacuo and the residuewas purified by prep-HPLC to give 65 as the indicated mixture ofdiastereoisomers (8.5 mg, 5%) as a white solid. LC-MS (Agilent): R_(t)3.47 min; m/z calculated for C₃₃H₃₅N₃O₄ [M+H]⁺ 538.3, found [M+H]⁺538.3. HPLC (JULY-L) (214 and 254 nm): R_(t) 8.50 min.

Example 24: Alternative Synthesis of Compound 65

1. Procedure for the Preparation of Compound 65f

To a stirred solution of diphenyl acetic acid (5.0 g, 23.5 mmol) in DCM(50 mL) at 0° C. was added CDI (4.6 g, 28.3 mmol) in portions and themixture was stirred at RT for 1 h, TLC (DCM:MeOH=20:1) showed thestarting material was consumed. The mixture was washed with water (30mL×2) and brine (30 mL×2), dried over Na₂SO₄, filtered and concentratedin vacuo to give 65f (5.6 g, 90%) as a white solid. LC-MS (Agilent):R_(t) 3.70 min; m/z calculated for C₁₇H₁₄N₂O [M+H]⁺ 263.1, found [M+H]⁺263.1.

2. Procedure for the Preparation of Compound 65

To a stirred solution of pure 65e (27 mg, 0.079 mmol) in DMF (1 mL) wasadded tetra methyl guanidine (9.3 mg, 0.081 mmol) under a N₂ atmosphereand the mixture was stirred at RT for 1 h. Compound 65f (25 mg, 0.094mmol) was added and stirring was continued at RT overnight. Morecompound 65f (24.7 mg, 0.094 mmol) was added stirring was continued atRT for another day. Water (10 mL) was added and the mixture was basifiedto pH 9 with K₂CO₃ and washed with ether. The aqueous layer was thenacidified to pH 3-4 with a 1 M aqueous HCl solution and extracted withCHCl₃/i-PrOH (v/v=3/1, 15 mL×3). The combined organic extracts wereconcentrated in vacuo and the residue was purified by prep-HPLC to give65 as the indicated mixture of diastereoisomers (7 mg, 16%) as a whitesolid. LC-MS (Agilent): R_(t) 3.41 min; m/z calculated for C₃₃H₃₅N₃O₄[M+H]⁺ 538.3, found [M+H]⁺ 538.3. HPLC (JULY-L) (214 and 254 nm): R_(t)8.50 min.

Example 25: Compound 70(2S,4S)-4-(2-benzylpiperidin-1-yl)-1-(2,2-diphenylacetyl)-pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of Compound 70a

A mixture of 2-benzyl pyridine (2.0 g, 1.08 mmol) and PtO₂ (200 mg, 0.72mmol) in AcOH (20 mL) was stirred at RT under a H₂ atmosphere (0.6 Mpa)for 6 h, TLC (PE:EA=4:1) showed the starting material was consumed. Themixture was filtered and the filtrate was concentrated in vacuo. Theresidue was partitioned between DCM (30 mL) and water (30 mL) and theaqueous layer was basified to pH 8-9 with K₂CO₃. The organic layer wasseparated, washed with brine (15 mL), dried over Na₂SO₄, filtered andconcentrated in vacuo to give 70a (1.9 g, 94%) as a colorless oil. LC-MS(Agilent): R_(t) 2.77 min; m/z calculated for C₁₂H₁₇N [M+H]⁺ 176.1,found [M+H]⁺ 176.2.

2. Procedure for the Preparation of Compound 706

To a stirred solution of compound 28a (900 mg, 2.67 mmol) and 2-benzylpiperidine (compound 70a) (468 mg 2.67 mmol) in DCE (10 mL) was addedAcOH (0.5 mL) and the mixture was stirred at RT for 30 min then cooledto 0° C. NaBH(OAc)₃ (849 mg, 4.01 mmol) was added and stirring wascontinued at RT overnight, TLC (PE:EA=1:1) showed most of the startingmaterial was consumed. The mixture was partitioned between DCM (20 mL)and a saturated aqueous NaHCO₃ solution (20 mL). The organic layer wasseparated, washed with brine, dried over Na₂SO₄, filtered andconcentrated in vacuo. The residue was purified by chromatography(DCM:EA=1:0 to 5:1) to give one diastereoisomer 70b-A (170 mg, 13%) as awhite solid. Further elution then gave the other diastereoisomer 70b-B(150 mg, 12%) as a white solid. The absolute stereochemistry of thesediastereoisomers was not determined and therefore are referred to as70-A and 70-B.

LCMS for Compound 70b-A

LC-MS (Agilent): R_(t) 3.42 min; m/z calculated for C₃₂H₃₆N₂O₃ [M+H]⁺497.3, found [M+H]⁺ 497.3.

LCMS for Compound 70b-B

LC-MS (Agilent): R_(t) 3.39 min; m/z calculated for C₃₂H₃₆N₂O₃ [M+H]⁺497.3, found [M+H]⁺ 497.3.

3. Procedure for the Preparation of Compound 70-A

To a stirred solution of compound 70b-A (170 mg, 0.34 mmol) in THF/water(5 mL/1 mL) at 0° C. was added LiOH.H₂O (36 mg, 0.85 mmol) and themixture was stirred at RT overnight, TLC (PE:EA=1:1) showed the startingmaterial was consumed. Most of the THF was removed in vacuo and theresidue was dissolved in water (15 mL), cooled in an ice-water bath andacidified to pH 3˜4 with a 1 M aqueous HCl solution. The resultingprecipitate was collected by filtration and re-crystallized from EA (20mL) to give 70-A (23 mg, 14%) as a white solid. LC-MS (Agilent): R_(t)3.51 min; m/z calculated for C₃₁H₃₄N₂O₃ [M+H]⁺ 483.3, found [M+H]⁺483.3. HPLC (214 and 254 nm): R_(t) 8.76 min.

4. Procedure for the Preparation of Compound 70-B

The hydrolysis reaction from 3. above was repeated for 70b-B (150 mg,0.30 mmol) and after acidification, the aqueous mixture was thenextracted with chloroform (15 mL×3) and the combined organic extractswere washed with brine (15 mL), dried over Na₂SO₄, filtered andconcentrated in vacuo to give 70-B (120 mg, 83%) as a thick oil. LC-MS(Agilent): R_(t) 3.68 min; m/z calculated for C₃₁H₃₄N₂O₃ [M+H]⁺ 483.3,found [M+H]⁺ 483.3. HPLC (JULY-L) (214 and 254 nm): R_(t) 8.96 min.

Example 26: Compound 55(2S,4R)-4-(2-(benzyloxy)ethyl)-1-(2,2-diphenylacetyl)-pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 28a

To a solution of 2b (7.00 g, 20.6 mol) in acetone (70 mL) at 0° C. wasadded Jones reagent (2.6 M, 9.00 mL, 28.9 mol) and the mixture wasallowed to warm to RT and stirred for 20 min, TLC (PE:EA=2:1) showed thestarting material was consumed. The reaction was quenched withisopropanol, Celite (3 g) was added and the mixture was filtered. Thefiltrate was concentrated in vacuo and the residue was partitionedbetween EA (40 mL) and water (40 mL). The layers were separated and theorganic phase was washed with a saturated aqueous NaHCO₃ solution (30mL), brine (30 mL×2) then dried over Na₂SO₄, filtered and concentratedin vacuo. The residue was purified by chromatography (PE:EA=1:0 to 2:1)to give 28a (5.95 g, 85%) as a white solid. LC-MS (Agilent, P-2): R_(t)2.79 min; m/z calculated for C₂₀H₁₉NO₄ [M+H]⁺ 338.1, found [M+H]⁺ 338.1.

2. Procedure for the Preparation of 55a

To a solution of benzyl 2-(diethoxyphosphoryl)acetate (1.68 g, 6.52mmol) in dry THF (10 mL) at 0° C. was added NaH (60% dispersion inmineral oil, 260 mg, 6.52 mmol) in portions and the mixture was stirredat 0° C. for 30 min. A solution of 28a (2.00 g, 5.93 mmol) in THF (10mL) was then added and stirring was continued at 0° C. for a further 40min, TLC (PE:EA=2:1) showed that the starting material was consumed. Thereaction was quenched with ice-water (40 mL) and the mixture wasextracted with EA (20 mL×2). The combined organic extracts were washedwith brine, dried over Na₂SO₄, filtered and concentrated in vacuo. Theresidue was purified by chromatography (PE:EA=1:0 to 5:1) to give thefirst eluting product 55a (1.0 g, 36%) and second eluting product 55b(1.8 g, 64%) as thick oils, which were assigned as Z and E isomersrespectively. LC-MS (Agilent, P-2) for 55a: R_(t) 3.02 min; m/zcalculated for C₂₉H₂₇NO₅ [M+H]⁺ 470.2, found [M+H]⁺ 470.2. LC-MS(Agilent, P-2) for 55b: R_(t) 3.01 min; m/z calculated for C₂₉H₂₇NO₅[M+H]⁺ 470.2, found [M+H]⁺ 470.2.

3. Procedure for the Preparation of 55c

A mixture of 55a (1.00 g, 2.1 mmol) and 10% Pd/C (100 mg) in MeOH (20mL) was stirred at RT under a, H₂ atmosphere (1 atm) overnight, TLC(PE:EA=2:1) showed that the starting material was consumed. The mixturewas filtered and the filtrate was concentrated in vacuo to give 55c(0.75 g, 87%) as a white solid. LC-MS (Agilent, P-2): R_(t) 2.70 min;m/z calculated for C₂₂H₂₃NO₅ [M+H]⁺ 382.1, found [M+H]⁺ 382.1.

4. Procedure for the Preparation of 55d

To a solution of 55c (0.70 g, 1.8 mmol) in dry THF (20 mL) at 0° C.under N₂ was added BH₃/THF (1 M solution in THF, 2.00 mL, 2.00 mmol) andthe mixture was stirred at 0° C. for 1 h, TLC (DCM:MeOH=10:1) showedthat the starting material was consumed. The reaction was quenched withMeOH (2 mL), a 3 M aqueous HCl solution (5 mL) was added and the mixturewas stirred at RT for 1 h then partitioned between EA and brine. Thelayers were separated and the organic phase was dried over Na₂SO₄,filtered and concentrated in vacuo. The residue was purified bychromatography (PE:EA=1:0 to 1:1) to give 55d (500 mg, 76%) as acolorless oil. LC-MS (Agilent, P-2): R_(t) 2.74 min; m/z calculated forC₂₂H₂₅NO₄ [M+H]⁺ 368.2, found [M+H]⁺ 368.2.

5. Procedure for the Preparation of 55e

To a solution of 55d (200 mg, 0.54 mmol) and benzyl2,2,2-trichloroacetimidate (151 mg, 0.59 mmol) in DCM (10 mL) at RT wasadded 1 drop of CF₃SO₃H and the mixture was stirred at RT overnight, TLC(DCM:MeOH=10:1) showed that the starting material was consumed. Themixture was washed with brine then dried over Na₂SO₄, filtered andconcentrated in vacuo. The residue was purified by chromatography(PE:EA=1:0 to 4:1) to give 55e (120 mg, 50%) as a colorless oil. LC-MS(Agilent, P-2): R_(t) 3.05 min; m/z calculated for C₂₉H₃₁NO₄[M+H]⁺458.2, found [M+H]⁺ 458.2.

6. Procedure for the Preparation of 55

A mixture of 55e (120 mg, 0.26 mmol) and LiOH.H₂O (33 mg, 0.78 mmol) inTHF/water (3 mL/1 mL) was stirred at RT overnight, TLC (PE:EA=2:1)showed that the starting material was consumed. Most of the THF wasremoved in vacuo and the residue was dissolved in water (20 mL),acidified to pH 3 with a 3 M aqueous HCl solution and extracted with DCM(20 mL×2). The combined organic extracts were washed with brine, driedover Na₂SO₄, filtered and concentrated in vacuo. The residue waspurified by preparative HPLC to give 55 (90 mg, 78%) as a white solid.LC-MS (Agilent, P-2): R_(t) 2.95 min; m/z calculated for C₂₈H₂₉NO₄[M+H]⁺ 444.2, found [M+H]⁺ 444.2. HPLC (JULY-L) (214 and 254 nm): R_(t)9.25 min.

Example 27: Compound 67(3R,4S)-1-(2,2-diphenylacetyl)-4-(methyl(3-phenylpropyl)amino)pyrrolidine-3-carboxylic acid and(3S,4R)-1-(2,2-diphenylacetyl)-4-(methyl(3-phenylpropyl)amino)pyrrolidine-3-carboxylic acid

1. Procedure for the Preparation of 67a

To a solution of(3R,4S)-methyl-1-benzyl-4-(tert-butoxycarbonyl)amino-pyrrolidine-3-carboxylate(500 mg, 1.49 mmol) in MeOH (20 mL) was added Pearlman's catalyst (50mg) and the mixture was stirred at RT under a H₂ atmosphere (1 atm)overnight, TLC (PE:EA=2:1) showed that the starting material wasconsumed. The mixture was filtered, the filtrate was concentrated invacuo and the residue was dissolved in DCM (20 mL). Diphenyl acetic acid(347 mg, 1.64 mmol) and EDCI.HCl (343 mg, 1.79 mmol) were added and themixture was stirred at RT overnight, TLC (DCM:MeOH=10:1) showed thestarting material was consumed. The mixture was washed with brine (15mL×2), dried over Na₂SO₄, filtered and concentrated in vacuo. Theresidue was purified by chromatography (PE:EA=1:0 to 4:1) to give 67a(150 mg, 23%) as a colorless oil. LC-MS (Agilent): R_(t) 4.37 min; m/zcalculated for C₂₅H₃₀N₂O₅ [M+H]⁺ 439.2, [M+Na]⁺ 461.2, found [M+H]⁺439.2, [M+Na]⁺ 461.2.

2. Procedure for the Preparation of 676

67a (150 mg, 0.34 mmol) was dissolved in a 4 M HCl/MeOH solution (10 mL)and the mixture was stirred at RT overnight, TLC (PE:EA=2:1) showed thatthe starting material was consumed. The mixture was concentrated invacuo and the residue was partitioned between DCM (20 mL) and water (15mL). The aqueous phase was basified to pH 9 with K₂CO₃ and the layerswere separated. The aqueous layer was further extracted with DCM (10mL×3) and the combined organic extracts were washed with brine, driedover Na₂SO₄, filtered and concentrated in vacuo to give 67b (130 mg,100%) as a colorless oil which was used directly in the next step. LC-MS(Agilent): R_(t) 4.13 min; m/z calculated for C₂₀H₂₂N₂O₃ [M+H]⁺ 339.2,found [M+H]⁺ 339.2.

3. Procedure for the Preparation of 67c

To solution of 67b (130 mg, 0.34 mmol) and 3-phenylpropanal (45 mg, 0.34mmol) in MeOH (10 mL) was added 1 drop of AcOH and the mixture wasstirred at RT for 0.5 h. NaCNBH₃ (28 mg, 0.44 mmol) was then added andstirring was continued at RT overnight, TLC (DCM:MeOH=10:1) showed thestarting material was consumed. The mixture was concentrated in vacuoand the residue was partitioned between DCM and brine. The organic layerwas collected, dried over Na₂SO₄, filtered and concentrated in vacuo.The residue was purified by chromatography (PE:EA=1:0 to 2:1) to give67c (120 mg, 77%) as a colorless oil. LC-MS (Agilent): R_(t) 3.85 min;m/z calculated for C₂₉H₃₂N₂O₃ [M+H]⁺ 457.2, found [M+H]⁺ 457.2.

4. Procedure for the Preparation of 67d

To solution of 67c (120 mg, 0.26 mmol) and 37% aqueous formaldehyde (25mg, 0.32 mmol) in MeOH (15 mL) at 0° C. was added 2 drops of AcOH andthe mixture was stirred at 0° C. for 30 min. NaCNBH₃ (20 mg, 0.32 mmol)was added and stirring was continued at RT overnight, TLC (PE:EA=2:1)showed that the starting material was consumed. The mixture wasconcentrated in vacuo and the residue was partitioned between water (10mL) and EA (20 mL). The layers were separated and the organic phase waswashed with brine (10 mL×2), dried over Na₂SO₄, filtered andconcentrated in vacuo. The residue was purified by chromatography(PE:EA=5:1 to 3:1) to give 67d (65 mg, 53%) as a colorless oil. LC-MS(Agilent): R_(t) 3.97 min; m/z calculated for C₃₀H₃₄N₂O₃ [M+H]⁺ 471.3,found [M+H]⁺ 471.3.

5. Procedure for the Preparation of 67

A mixture of 67d (65 mg, 0.14 mmol) and LiOH.H₂O (18 mg, 0.41 mmol) inTHF/water (10 mL/2 mL) was stirred at RT overnight, TLC (PE:EA=2:1)showed the starting material was consumed. Most of the THF was removedin vacuo and the residue was dissolved in water H₂O (10 mL), acidifiedto pH 4˜5 with a 3 M aqueous HCl solution and extracted with DCM (10mL×2). The combined organic extracts were washed with brine (15 mL),dried over Na₂SO₄, filtered and concentrated in vacuo. The residue waspurified by preparative HPLC to give 67 (40 mg, 63%) as a white solid.LC-MS (Agilent): R_(t) 3.78 min; m/z calculated for C₂₈H₃₀N₂O₃ [M+H]⁺457.3, found [M+H]⁺ 457.3. HPLC (JULY-L) (214 and 254 nm): R_(t) 8.79min.

Example 28: Compound 75(2S,4S)-1-(2,2-diphenylacetyl)-4-(1-oxo-3-phenyl-2,7-diazaspiro[3,5]nonan-7-yl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 75a

tert-Butyl 1-oxo-3-phenyl-2,7-diazaspiro[3.5]nonane-7-carboxylate (300mg, 0.94 mmol) was added to a 4 M HCl/MeOH solution (5 mL) at 0° C. andthe mixture was stirred at RT for 3 h, after which time a whitesuspension formed. LCMS analysis showed that the starting material wasconsumed. EA (3 mL) and diethyl ether (10 mL) were added and the solidmaterial was collected by filtration, washed with diethyl ether (5 mL×2)and dried to give 75a (280 mg, >100%) as a white solid, which was usedin the following step without further purification. LC-MS (Agilent):R_(t) 2.75 min; m/z calculated for C₁₃H₁₆N₂O [M+H]⁺ 217.1, found [M+H]⁺217.1.

2. Procedure for the Preparation of 75b

A solution of 28a (100 mg, 0.29 mmol), 75a (75 mg, 0.29 mmol) and Et₃N(33 mg, 0.32 mmol) in MeOH (10 mL) was stirred at RT for 30 min beforeadding 1 drop of AcOH and NaCNBH₃ (20 mg, 0.32 mmol). The mixture wasthen allowed to stir at RT overnight, TLC (PE:EA=1:1) showed that thestarting material was consumed and 75b was confirmed by LCMS analysis.The reaction was repeated on a larger amount of 75a (200 mg, 0.59 mmol)and the two reaction mixtures were combined and concentrated in vacuo.The residue was dissolved in DCM (30 mL), washed with brine (30 mL) thendried over Na₂SO₄, filtered and concentrated in vacuo. Purification bycolumn chromatography (DCM:MeOH=1:0 to 20:1) gave 75b (60 mg, 12%) as acolorless oil. LC-MS (Agilent): R_(t) 3.41 min; m/z calculated forC₃₃H₃₅N₃O₄ [M+H]⁺ 538.3, [M+Na]⁺ 560.3, found [M+H]⁺ 538.3, [M+Na]⁺560.3.

3. Procedure for the Preparation of Compound 75

To a mixture of 75b (60 mg, 0.11 mmol) in THF/water (5 mL/1 mL) wasadded LiOH.H₂O (14 mg, 0.33 mmol) and the mixture was stirred at RTovernight, TLC (DCM:MeOH=10:1) showed that the starting material wasconsumed. Most of THF was removed in vacuo and the residue was dissolvedin water (20 mL), acidified to pH 3-4 with a 3 M aqueous HCl solutionand extracted with DCM (15 mL×3). The combined organic extracts werewashed with brine, dried over Na₂SO₄, filtered and concentrated in vacuoto give 50 mg of crude product which was suspended in EA (5 mL). Theobtained mixture was heated at reflux for 30 min, cooled to RT and theprecipitate was collected by filtration then dried to give 75 (25 mg,43%) as a white solid. LC-MS (Agilent): R_(t) 3.67 min; m/z calculatedfor C₃₂H₃₃N₃O₄ [M+H]⁺ 524.3, found [M+H]⁺ 524.3. HPLC (214 and 254 nm):R_(t) 8.53 min.

Example 29: Compound 76(2R,4R)-1-(2,2-diphenylacetyl)-4-(3-phenylpropoxy)-pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of Compound 76a

cis-4-Hydroxy-D-proline was prepared using the procedure described inTetrahedron Asymmetry, 2002, 13, 197. To a solution ofcis-4-Hydroxy-D-proline (20 g, 0.15 mol) in MeOH (200 mL) at 0° C. wasadded SOCl₂ (19.9 g, 0.17 mol) dropwise and the mixture was then heatedat 70° C. overnight, LCMS analysis showed that the starting material wasconsumed. The mixture was cooled to RT and concentrated in vacuo to give76a (22 g, 100%) as brown solid. LC-MS (Agilent): R_(t) 0.64 min; m/zcalculated for C₆H₁₁NO₃ [M+H]⁺ 146.1, found [M+H]⁺ 146.1.

2. Procedure for the Preparation of 76b

To a solution of diphenylacetic acid (15.9 g, 75.2 mmol) in DCM (150 mL)at 0° C. was added DMF (2 drops) and SOCl₂ (11.6 g, 87.7 mmol) and themixture was heated at reflux for 2 h. The solvent was removed in vacuoand the residue was dissolved in ether (20 mL) and added slowly to amixture of 76a (15 g, 83 mmol) and K₂CO₃ (15.6 g, 113 mmol) in water(250 mL) and ether (100 mL) at 0° C. The mixture was stirred at 0° C.for 2 h, TLC (PE:EA=1:1) showed a major new product was formed. Thelayers were separated and the aqueous layer was extracted with EA (80mL×2). The combined organic extracts were washed with brine, dried overNa₂SO₄, filtered and concentrated in vacuo. The residue was purified bycolumn chromatography (PE:EA=10:1 to 3:1) to give 76b (20 g, 80%)′ as ayellow solid. LC-MS (Agilent): R₁ 3.53 min; m/z calculated for C₂₀H₂₁NO₄[M+H]⁺ 340.1 found [M+H]⁺ 340.1.

3. Procedure for the Preparation of 76c

To a stirred solution of 76b (1.0 g, 2.9 mmol) and cinnamyl bromide(0.87 g, 4.4 mmol) in DMF (20 mL) −40° C. was added t-BuONa (0.28 g, 2.9mmol) in portions and the mixture was stirred at −40° C. for 2 h, TLC(PE:EA=1:1) showed that the starting material was consumed. The mixturewas allowed to warm to 0° C., water (100 mL) was added and extractedwith EA (30 mL×2). The combined organic extracts were washed with water(20 mL), brine (20 mL×2), dried over Na₂SO₄, filtered and concentratedin vacuo. The residue was purified by column chromatography (PE:EA=10:1to 3:1) to give 76c (0.8 g, 62%) as a white solid. LC-MS (Agilent):R_(t) 4.03 min; m/z calculated for C₂₉H₂₉NO₄ [M+H]⁺ 456.2, found [M+H]⁺456.1.

4. Procedure for the Preparation of 76d

To a solution of 76c (400 mg, 0.88 mmol) in MeOH (15 mL) was added 10%Pd/C (40 mg) and the mixture was stirred at RT under a H₂ atmosphere (1atm) overnight, TLC (PE:EA=2:1) showed that the starting material wasconsumed. The mixture was filtered through Celite and the filtrate wasconcentrated in vacuo to give 76d (370 mg, 92%) as a colorless oil.LC-MS (Agilent): R_(t) 4.12 min; m/z calculated for C₂₉H₃₁NO₄ [M+H]⁺458.2, found [M+H]⁺ 458.2.

5. Procedure for the Preparation of Compound 76

To a stirred solution of 76d (370 mg, 0.8 mmol) in THF/H₂O (10 mL/3 mL)was added LiOH.H₂O (102 mg, 2.4 mmol) and the mixture was heated at 30°C. overnight, TLC (PE:EA=2:1) showed that the starting material wasconsumed. Most of the THF was removed in vacuo and the residue wasdissolved in water (20 mL) and washed with Et₂O (15 mL×2). DCM (15 mL)was added and the aqueous layer was acidified to pH 2-3 with a 3 Maqueous HCl solution. The layers were separated and the aqueous layerwas further extracted with DCM (15 mL). The combined organic extractswere washed with brine, dried over Na₂SO₄, filtered and concentrated invacuo to give compound 76 (300 mg, 85%) as a white solid. LC-MS(Agilent): R_(t) 3.99 min; m/z calculated for C₂₈H₂₉NO₄ [M+H]⁺ 444.2,found [M+H]⁺ 444.2. HPLC (214 and 254 nm): R_(t) 9.36 min.

Example 30: Compound 90(2S,4S)-1-(2,2-diphenylacetyl)-4-(methyl(4-phenylbutyl)-amino)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 90a

To a stirred solution of 63b (100 mg, 0.29 mmol) and benzaldehyde (25mg, 0.24 mmol) in MeOH (5 mL) under nitrogen was added 2 drops of AcOHand the mixture was stirred for 1 h then cooled to 0° C. NaCNBH₃ (22 mg,035 mmol) was added and the mixture was allowed to warm slowly to RT andstirred overnight, TLC (DCM:MeOH=10:1) showed that most of the startingmaterial was consumed. Most of the MeOH was removed in vacuo, water (15mL) was added and the mixture was extracted with EA (15 mL×2). Thecombined organic extracts were washed with brine, dried over Na₂SO₄ andconcentrated in vacuo to give the crude 90a (150 mg) as a yellow oil.The procedure was repeated and the crude batches were combined andpurified by column chromatography (PE:EA=10:1 to 1:1) to give 90a (2.0g, 66%) as a white solid. LC-MS (Agilent): R_(t) 3.42 min; m/zcalculated for C₂₇H₂₈N₂O₃ [M+H]⁺ 429.2, found [M+H]⁺ 429.2.

2. Procedure for the Preparation of 90b

To a stirred solution of 90a (2.00 g, 4.67 mmol) and formaldehyde(37˜40% solution in water, 0.56 g, 7.01 mmol) in MeOH (40 mL) undernitrogen was added 3 drops of AcOH and the mixture was stirred for 1 hthen cooled to 0° C. NaCNBH₃ (0.35 g, 5.60 mmol) was added and themixture was allowed to warm slowly to RT and stirred overnight, TLC(DCM:MeOH=20:1) showed that most of the starting material was consumed.Most of the MeOH was removed in vacuo, water (20 mL) was added and themixture was extracted with DCM (30 mL). The organic layer was washedwith brine (25 mL), dried over Na₂SO₄ and concentrated in vacuo. Theresidue was purified by chromatography (PE:EA=10:1 to 4:1) to give 90b(1.86 g, 90%) as a white solid. LC-MS (Agilent): R_(t) 3.50 min; m/zcalculated for C₂₈H₃₀N₂O₃[M+H]⁺ 443.3, found [M+H]⁺ 443.3.

3. Procedure for the Preparation of 90c

A mixture of 90b (1.86 g, 4.20 mmol) and 10% Pd/C (200 mg) in MeOH (30mL) was stirred at RT under a H₂ atmosphere (1 atm) for 2 days, TLC(DCM:MeOH=10:1) showed that the starting material was consumed. Themixture was filtered and the filtrate was concentrated in vacuo to give90c (1.40 g, 95%) as colorless oil. LC-MS (Agilent): R_(t) 3.34 min; m/zcalculated for C₂₁H₂₄N₂O₃ [M+H]⁺ 353.2, found [M+H]⁺ 353.2.

4. Procedure for the Preparation of 90d

To a solution of 4-phenyl-1-butanol (0.5 g, 3.3 mmol) in DCM (10 mL) wasadded Celite (0.5 g) followed by PCC (1.8 g, 8.3 mmol) and the mixturewas stirred at RT for 3 h, TLC (PE:EA=2:1) showed that the startingmaterial was consumed. The mixture was filtered through a short plug ofsilica gel using DCM to wash. The filtrate was concentrated in vacuo togive 90d (0.5 g, 100%) as a yellow oil.

5. Procedure for the Preparation of 90e

To a stirred solution of 90c (202 mg, 0.57 mmol) and the aldehyde 90d(102 mg, 0.68 mmol) in MeOH (10 mL) at RT was added AcOH (1 drop) andthe mixture was stirred for 1 h then cooled to at 0° C. NaCNBH₃ (43 mg,0.68 mmol) was added and the mixture was allowed to warm to RT andstirred overnight, TLC (DCM:MeOH=20:1) showed that the starting materialwas consumed. The mixture was concentrated in vacuo and the residue wasdissolved in water (15 mL) and extracted with DCM. The organic extractswere washed with brine (15 mL×2), dried over Na₂SO₄, filtered andconcentrated in vacuo. Purification by column chromatography (PE:EA=4:1to 1:1) gave 90e (198 mg, 71%) as thick colorless oil. LC-MS (Agilent):R_(t) 3.61 min; m/z calculated for C₃₁H₃₆N₂O₃ [M+H]⁺ 485.3, found [M+H]⁺485.3.

6. Procedure for the Preparation of Compound 90

Hydrolysis of 90e (198 mg, 0.41 mmol) was performed as described inExample 27, 5. with 3 equivalents of LiOH.H₂O (52 mg, 1.23 mmol) and themixture was stirred at RT overnight, TLC (DCM: MeOH=20:1). The combinedorganic extracts were washed with brine (10 mL×2), dried over Na₂SO₄,filtered and concentrated in vacuo to give 90 (185 mg, 96%) as whitesolid. LC-MS (Agilent): R_(t) 3.67 min; m/z calculated for C₃₁H₃₆N₂O₃[M+H]⁺ 471.3, found [M+H]⁺ 471.3. HPLC (214 and 254 nm): R_(t) 8.93 min.

Example 31: Compound 91(2S,4S)-1-(2,2-diphenylacetyl)-4-((3-(4-fluorophenyl)-propyl)(methyl)amino)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 91a

To a solution of the alcohol (1.0 g, 6.5 mmol) in DCM (20 mL) was addedCelite (1.5 g) and PCC (3.5 g, 16.2 mmol) and the mixture was stirred atRT for 3 h. TLC (PE:EA=4:1) showed the starting material was consumed.The mixture was charged on to a silica column and flushed with DCM togive 91a (0.8 g, 79%) as a yellow oil, which was used directly in thenext step.

2. Procedure for the Preparation of 91b

To a solution of 63b (113 mg, 0.33 mmol) and 91a (41 mg 0.27 mmol) inMeOH (10 mL) at 0° C. under a N₂ atmosphere was added a drop of AcOH andthe mixture was stirred for 30 min. NaCNBH₃ (21 mg, 0.33 mmol) was thenadded and the mixture was allowed to warm slowly to RT and stirredovernight, TLC (DCM:MeOH=10:1) showed most of starting material wasconsumed. The mixture was concentrated in vacuo to give crude 91b (150mg) as a yellow oil. The reaction was repeated on a larger batch of 63b(509 mg, 1.5 mmol) and the crude products were combined and purified bycolumn chromatography (DCM:MeOH=50:1 to 20:1) to give 91b (500 mg, 57%)as a white solid. LC-MS (Agilent): R_(t) 3.37 min; m/z calculated forC₂₉H₃₁FN₂O₃ [M+H]⁺ 475.2, found [M+H]⁺ 475.3.

3. Procedure for the Preparation of 91c

To a solution of 91b (210 mg, 0.44 mmol) and formaldehyde (37% aqueoussolution, 72 mg, 0.88 mmol) in MeOH (10 mL) at 0° C. under a N₂atmosphere was added 2 drops of AcOH and the mixture was stirred for 30min. NaCNBH₃ (56 mg, 0.88 mmol) was then added and the mixture wasallowed to warm slowly to RT and stirred overnight, TLC (DCM:MeOH=10:1)showed the starting material was consumed. The mixture was concentratedin vacuo and the residue was dissolved in EA (15 mL), washed with water(10 mL), saturated aqueous NaHCO₃ solution (15 mL), brine (15 mL) anddried over Na₂SO₄. The solvent was removed in vacuo and the residue waspurified by column chromatography (DCM:MeOH=100:1 to 50:1) to give 91c(170 mg, 79%) as a colorless oil. LC-MS (Agilent): R_(t) 3.76 min; m/zcalculated for C₃₀H₃₃FN₂O₃ [M+H]⁺ 489.3, found [M+H]⁺ 489.3.

4. Procedure for the Preparation of Compound 91

Hydrolysis of 91c (170 mg, 0.35 mmol) was performed using the procedureof Example 9, 3. with about 3 equivalents of LiOH.H₂O (44 mg, 1.04 mmol)at RT and the mixture was stirred overnight, TLC (MeOH:DCM=1:10) showedthe starting material was consumed. Most of the THF was removed in vacuoand the residue was dissolved in water (15 mL) and washed with Et₂O (10mL×2). The aqueous layer was acidified to pH 2-3 with a 3 M aqueous HClsolution and the resulting precipitate was collected by filtration anddried to give 91 (90 mg, 54%) as a white solid. LC-MS (Agilent): R_(t)3.52 min; m/z calculated for C₂₉H₃₁FN₂O₃ [M+H]⁺ 475.2, found [M+H]⁺475.3. HPLC (214 and 254 nm): R_(t) 8.86 min.

Example 32: Compound 93(2S,4S)-1-(2,2-diphenylacetyl)-4-(methyl(3-pyridinyl)-propyl)amino)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 93a

To a solution of 3-(pyridin-3-yl)propan-1-ol (500 mg, 3.6 mmol) in DCM(10 mL) was added Dess-Martin reagent (1.7 g, 4.0 mmol) and the mixturewas stirred at RT overnight, TLC (DCM:MeOH=10:1) showed that thestarting material was consumed. Water (20 mL) was added and the solidwas removed by filtration. The filtrate layers were separated and theaqueous layer was extracted with DCM (15 mL). The combined organicslayers were washed with brine, dried over Na₂SO₄, filtered andconcentrated in vacuo. The residue was purified by chromatography(DCM:MeOH=150:0 to 50:1) to give 93a (200 mg, 40%) as a white solid.LC-MS (Agilent): R_(t) 0.58 min; m/z calculated for C₈H₉NO [M+H]⁺ 136.1,found [M+H]⁺ 136.1.

2. Procedure for the Preparation of 93b.

To a solution of 93a (57 mg, 0.42 mmol) and 90c (100 mg, 0.28 mmol) inMeOH (10 mL) was added 2 drops of AcOH and the mixture was stirred at RTfor 1 h. NaCNBH₃ (27 mg, 0.42 mmol) was added and stirring was continuedat RT overnight, TLC (DCM:MeOH=10:1) showed that the starting materialwas consumed. The mixture was concentrated in vacuo and the residuesuspended in water (20 mL) and extracted with EA (15 mL×2). The combinedorganic extracts were washed with brine, dried over Na₂SO₄, filtered andconcentrated in vacuo. The residue was purified by chromatography(DCM:MeOH=100:1 to 50:1) to give 93b (100 mg, 75%) as a yellow oil.LC-MS (Agilent): R_(t) 3.52 min; m/z calculated for C₂₉H₃₃N₃O₃ [M+H]⁺472.3, found [M+H]⁺ 472.3.

3. Procedure for the Preparation of Compound 93

A mixture of 93b (100 mg, 0.21 mmol) and LiOH.H₂O (18 mg, 0.42 mmol) inTHF/water (6 mL/2 mL) was stirred at RT overnight, TLC (DCM:MeOH=10:1)showed that the starting material was consumed. Most of the THF wasremoved in vacuo and the residue was dissolved in water (15 mL) andwashed with ether (10 mL). The aqueous layer was acidified to pH 5 witha 3 M aqueous HCl solution and freeze dried to give a white solid, whichwas suspended in DCM/MeOH and filtered. The filtrate was concentrated invacuo and the residue was purified by preparative HPLC to give 93 (70mg, 74%) as a white solid. LC-MS (Agilent): R_(t) 3.59 min; m/zcalculated for C₂₈H₃₁N₃O₃ [M+H]⁺ 458.2, found [M+H]⁺ 458.2. HPLC(JULY-L) (214 and 254 nm): R_(t) 8.33 min.

Example 33: Compound 94(2S,4S)-4-cinnamamido-1-(2,2-diphenylacetyl)-pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 94a

To a solution of 63b (1.05 g, 3.1 mmol) and cinnamic acid (0.46 g, 3.10mmol) in DCM (40 mL) at RT under nitrogen was added EDCI.HCl (0.65 g,3.39 mmol) and the mixture was stirred overnight, TLC (DCM:MeOH=10:1)showed the reaction was complete. The mixture was washed with brine (20mL×2), dried over Na₂SO₄, filtered and concentrated in vacuo. Theresidue was purified by column chromatography (PE:EA=1:0 to 1:1) to give94a (1.28 g, 88%) as a white solid. LC-MS (Agilent): R_(t) 3.84 min;in/z calculated for C₂₉H₂₈N₂O₄ [M+H]⁺ 469.2, [M+Na]⁺ 491.2, found [M+H]⁺469.2, [M+Na]⁺ 491.2.

2. Procedure for the Preparation of Compound 94

To a mixture of 94a (300 mg, 0.64 mmol) in THF/H₂O (15 mL/2 mL) wasadded LiOH.H₂O (81 mg, 1.92 mmol) and the mixture was stirred at RTovernight, TLC (DCM:MeOH=10:1) showed the starting material wasconsumed. Most of the THF was removed in vacuo and the residue wasdissolved in water H₂O (20 mL), acidified to pH 2-3 with a 3 M aqueousHCl solution and extracted with DCM (25 mL×2). The combined organicextracts were washed with brine (20 mL), dried over Na₂SO₄, filtered andconcentrated in vacuo to give 94 (286 mg, 98%) as a white solid. LC-MS(Agilent): R_(t) 3.71 min; m/z calculated for C₂₈H₂₆N₂O₄ [M+H]⁺ 455.2,found [M+H]⁺ 455.2. HPLC (214 and 254 nm): R_(t) 9.08 min.

Example 34: Compound 95(2S,4S)-1-(2,2-diphenylacetyl)-4-(N-methylcinnamamido)-pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 95a

To a stirred solution of 90c (300 mg, 0.85 mmol) and cinnamic acid (126mg, 0.85 mmol) in DCM (15 mL) at RT under nitrogen was added EDCI.HCl(180 mg, 0.94 mmol) and the mixture was stirred overnight, TLC(DCM:MeOH=10:1) showed that the starting material was consumed. Themixture was washed with a saturated aqueous NaHCO₃ solution (15 mL×2), a0.5 M aqueous HCl solution (15 mL×2), brine (15 mL×2), dried over Na₂SO₄and filtered. The solvent was removed in vacuo and the residue waspurified by column chromatography (PE:EA=2:1) to give 95a (300 mg, 73%)as a white solid. LC-MS (Agilent): R_(t) 3.93 min; m/z calculated forC₃₀H₃₀N₂O₄ [M+H]⁺ 483.2, [M+Na]⁺ 505.2, found [M+H]⁺ 483.2, [M+Na]⁺505.2.

2. Procedure for the Preparation of 95

To a stirred solution of 95a (300 mg, 0.62 mmol) in THF/water (15 mL/2mL) was added LiOH.H₂O (78 mg, 1.87 mmol) and the mixture was stirred atRT overnight, TLC (DCM:MeOH=10:1) showed the starting material wasconsumed. Most of the THF was removed in vacuo and the residue wasdissolved in water (20 mL). The solution was acidified to pH-3˜4 with a3 M aqueous HCl solution and extracted with EA (15 mL×2). The combinedorganic extracts were washed with brine (20 mL), dried over Na₂SO₄,filtered and concentrated in vacuo to give 95 (270 mg, 93%) as a whitesolid. LC-MS (Agilent): R_(t) 3.88 min; m/z calculated for C₂₉H₂₈N₂O₄[M+H]⁺ 469.2, [M+Na]⁺ 491.2, found [M+H]⁺ 469.2, [M+Na]⁺ 491.2. HPLC(214 and 254 nm): R_(t) 9.12 min.

Example 35: Compound 96(2S,4S)-1-(2,2-diphenylacetyl)-4-(3-phenylpropanamido)-pyrrolidine-2-carboxylicacid

To a solution of 94 (170 mg, 0.37 mmol) in EA (30 mL) was added 10% Pd/C(20 mg) and the mixture was stirred at RT under a H₂ atmosphere (1 atmpressure) overnight, TLC (DCM:MeOH=10:1) showed the starting materialwas consumed. The mixture was filtered and the filtrate was concentratedin vacuo to give 96 (150 mg, 88%) as a white solid. LC-MS (Agilent):R_(t) 3.80 min; m/z calculated for C₂₈H₂₈N₂O₄ [M+H]⁺ 457.2, [M+Na]⁺479.2, found [M+H]⁺ 457.2, [M+Na]⁺ 479.2. HPLC (214 and 254 nm): R_(t)9.06 min.

Example 36: Compound 97(2S,4S)-1-(2,2-diphenylacetyl)-4-(N-methyl-3-phenylpropanamido)pyrrolidine-2-carboxylicacid

To a mixture of 95 (80 mg, 0.17 mmol) and 10% Pd/C (20 mg) in H₂O (20mL) was added NaOH (10 mg, 0.26 mmol) and the mixture was stirred at RTunder a H₂ atmosphere (1 atm pressure) overnight, LCMS analysis showedthe starting material was consumed. The mixture was filtered and thefiltrate was acidified to pH=3˜4 with a 3 M aqueous HCl solution andextracted with EA (10 mL×3). The combined organic extracts were washedwith brine (20 mL×2), dried over Na₂SO₄ and concentrated in vacuo. Theresidue was re-crystallized from Et₂O to give 97 (15 mg, 19%) as a whitesolid. LC-MS (Agilent): R_(t) 3.86 min; m/z calculated for C₂₉H₃₀N₂O₄[M+H]⁺ 471.2, [M+Na]⁺ 493.2, found [M+H]⁺ 471.2, [M+Na]⁺ 493.2. HPLC(214 and 254 nm): R_(t) 9.12 min.

Example 37: Compound 98(2S,4S)-1-(2,2-diphenylacetyl)-4-(N-3-phenylpropyl)-acetamido)pyrrolidine-2-carboxylicacid 1. Procedure for the preparation of 98a

To a solution of 63b (500 mg, 1.5 mmol) and 3-phenylpropanal (161 mg,1.2 mmol) in MeOH (10 mL) at RT was added AcOH (2 drops) and the mixturewas stirred for 1 h. The mixture was cooled to 0° C., NaCNBH₃ (113 mg,1.8 mmol) was added and stirring was continued at RT overnight, TLC(DCM:MeOH=20:1) showed that the starting material was consumed. Most ofthe MeOH was removed in vacuo and the residue was partitioned betweenwater (20 mL) and EA (15 mL). The layers were separated and the aqueousphase was further extracted with EA (20 mL). The combined organicextracts were washed with brine, dried over Na₂SO₄, filtered andconcentrated in vacuo. The residue was purified by column chromatography(DCM:MeOH=100:1 to 50:1) to give 98a (320 mg, 58%) as a yellow oil.LC-MS (Agilent): R_(t) 3.46 min; m/z calculated for C₂₉H₃₄N₂O₃ [M+H]⁺457.3, found [M+H]⁺ 457.3.

2. Procedure for the Preparation of 98b

To a solution of 98a (150 mg, 0.33 mmol) in DCM (5 mL) at 0° C. wasadded Et₃N (40 mg, 0.4 mmol) followed by acetyl chloride (28 mg, 0.36mmol). The mixture was then stirred at RT for 15 min, TLC(DCM:MeOH=20:1) showed that the starting material was consumed. Themixture was washed with brine (10 mL×2) and the organic layer wasconcentrated in vacuo. Purification by column chromatography (PE:EA=4:1to 1:1) gave 98b (130 mg, 79%) as a yellow oil. LC-MS (Agilent): R_(t)3.89 min; m/z calculated for C₃₁H₃₄N₂O₄ [M+Na]⁺ 521.25, found [M+Na]⁺521.3.

3. Procedure for the Preparation of Compound 98

Hydrolysis of 98b (130 mg, 0.26 mmol) was performed as described inExample 5, 3. using 3 equivalents of LiOH.H₂O (32 mg, 0.78 mmol) to give98 (100 mg, 80%) as a light yellow solid. LC-MS (Agilent): R₁ 3.85 min;m/z calculated for C₃₀H₃₂N₂O₄ [M+H]⁺ 485.25, found [M+H]⁺ 485.3. HPLC(214 and 254 nm): R_(t) 9.19 min.

Example 38: Compound 99(2S,4S)-1-(2,2-diphenylacetyl)-4-(N-(3-phenylpropyl)-methylsulfonamido)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 99a

To a cooled mixture of 98a (150 mg, 0.33 mmol) in DCM (5 mL) and TEA (40mg, 0.4 mmol) at 0° C., was added MSCl (41 mg, 0.36 mmol). The mixturewas stirred at RT for 15 min. TLC (DCM:MeOH=20:1) showed that 99a haddisappeared, and the mixture was washed with brine. The organic phasewas dried over Na₂SO₄, and evaporated in vacuo. The resulting mixturewas purified by silica column (PE:EA=4:1 to 2:1) to give 99a (140 mg,79%) as white solid. LC-MS (Agilent): R_(t) 3.86 min; m/z calculated forC₃₀H₃₄N₂O₅S [M+H]⁺ 535.24, found [M+H]⁺ 535.3.

2. Procedure for the Preparation of Compound 99

Hydrolysis of 99a (140 mg, 0.26 mmol) was performed as described inExample 25, 3. with about 3 equivalents of LiOH.H₂O (33 mg, 0.79 mmol).The precipitate was collected by filter, washed with water (5 mL×2),dried at 50° C. overnight to give 99 (120 mg, 88%) as a white solid.LC-MS (Agilent): R_(t) 3.87 min; m/z calculated for C₂₉H₃₂N₂O₅S [M+H]⁺521.2, [M+Na]⁺ 543.2, found [M+H]⁺ 521.3, [M+Na]⁺ 543.2. HPLC (214 and254 nm): R_(t) 9.15 min.

Example 39: Compound 100(2S,4S)-1-(2,2-diphenylacetyl)-4-(5-phenyl-1H-1,2,3-triazol-1-yl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 100b

A mixture of 100a (100 mg, 0.27 mmol), phenyl acetylene (42 mg, 0.41mmol) and Cp*Ru(COD)Cl (10 mg, 0.027 mmol) in toluene (5 mL) was heatedat 80° C. under a N₂ atmosphere overnight, TLC (PE:EA=1:1) showed thatthe starting material was consumed. The mixture was cooled to RT,concentrated in vacuo and the residue was purified by columnchromatography (PE:EA=1:0 to 1:1) to give 100b (130 mg, 100%) as a whitesolid. LC-MS (Agilent): R_(t) 3.80 min; m/z calculated for C₂₈H₂₆N₄O₃[M+H]⁺ 467.2, [M+Na]⁺ 489.2, found [M+H]⁺ 467.2, [M+Na]⁺ 489.2.

2. Procedure for the Preparation of 100

To a mixture 100b (130 mg, 0.28 mmol) in THF/water (10 mL/1.5 mL) wasadded LiOH.H₂O (35 mg, 0.84 mmol) and the mixture was stirred at RTovernight, TLC (DCM:MeOH=10:1) showed that the starting material wasconsumed. Most of the THF was removed in vacuo and the residue wasdissolved in water (15 mL). The aqueous mixture was acidified to pH=5-6with a 3 M aqueous HCl solution and extracted with DCM (20 mL×2). Thecombined organic extracts were washed with brine, dried over Na₂SO₄,filtered and concentrated in vacuo to give 100 (120 mg, 95%) as a whitesolid. LC-MS (Agilent): R_(t) 3.87 min; m/z calculated for C₂₇H₂₄N₄O₃[M+H]⁺ 453.2, [M+Na]⁺ 475.2, found [M+H]⁺ 453.2, [M+Na]⁺ 475.2. HPLC(214 and 254 nm): R_(t) 8.98 min.

Example 40: Compound 101(2S,4S)-4-(5-benzyl-1H-1,2,3-triazol-1-yl)-1-(2,2-diphenylacetyl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 101a

A mixture of 100a (100 mg, 0.27 mmol), 1-(prop-2-ynyl)benzene (48 mg,0.41 mmo) and Cp*Ru(COD)Cl (10 mg, 0.027 mmol) in toluene (5 mL) washeated at 80° C. under a N₂ atmosphere overnight, TLC (PE:EA=1:1) showedthat the starting material was consumed. The reaction was cooled to RTand concentrated in vacuo to give 140 mg of crude product. The reactionwas repeated and the two batches of crude product were combined andpurified by column chromatography (PE:EA=1:0 to 1:1) to give 101a (230mg, 88%) as a white solid. LC-MS (Agilent): R_(t) 3.89 min; m/zcalculated for C₂₉H₂₈N₄O₃ [M+H]⁺ 481.2, [M+Na]⁺ 503.2, found [M+H]⁺481.2, [M+Na]⁺ 503.2.

2. Procedure for the Preparation of 101

Hydrolysis of 101a (230 mg, 0.48 mmol) was performed as described inExample 39, 2. using about 3 equivalents of LiOH.H₂O (64 mg, 1.53 mmol)to give 101 (190 mg, 97%) as a white solid. LC-MS (Agilent): R_(t) 3.82min; m/z calculated for C₂₈H₂₆N₄O₃ [M+H]⁺ 467.2, [M+Na]⁺ 489.2, found[M+H]⁺ 467.2, [M+Na]⁺ 489.2. HPLC (214 and 254 nm): R_(t) 9.00 min.

Example 41: Compound 102(2S,4S)-4-((S)-3-benzyl-5-oxomorpholino)-1-(2,2-diphenylacetyl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 102a.

To a solution of 28a (980 mg, 2.90 mmol) and L-phenylglycinol (483 mg,3.20 mmol) in MeOH (20 mL) at RT under N₂ was added AcOH (one drop) andthe mixture was stirred for 1 h then cooled to 0° C. NaCNBH₃ (219 mg,3.49 mmol) was added and the mixture was allowed to warm to RT andstirred overnight, TLC (DCM:MeOH=10:1) showed that the starting materialwas consumed. The mixture was concentrated in vacuo and the residue wasdissolved in water (20 mL) and extracted with DCM (25 mL). The organiclayer was washed with brine (15 mL×2), dried over Na₂SO₄, filtered andconcentrated in vacuo. The residue was purified by column chromatography(DCM:EA=3:1 to 1:1) to give 102a (395 mg, 29%) as a white solid. LC-MS(Agilent): R_(t) 3.47 min; m/z calculated for C₂₉H₃₂N₂O₄[M+H]⁺ 473.3,found [M+H]⁺ 473.3.

2. Procedure for the Preparation of 102b.

To a stirred solution of 102a (385 mg, 0.83 mmol) and Et₃N (101 mg, 1.00mmol) in THF (15 mL) at 0° C. was added chloroacetyl chloride (95 mg,0.83 mmol) and the mixture was allowed to warm to RT and stirredovernight, TLC (PE:EA=1:1) showed that the starting material wasconsumed. Most of the THF was removed in vacuo and the residue wasdiluted with water (15 mL) and extracted with EA (15 mL×2). The combinedorganic extracts were washed with brine (20 mL), dried over Na₂SO₄,filtered and concentrated in vacuo. The residue was purified by columnchromatography (PE:EA=10:1 to 3:2) to give 102b (190 mg, 43%) as a whitesolid. LC-MS (Agilent): R_(t) 3.83 min; in/z calculated forC₃₁H₃₃N₂O₅[M+H]⁺ 549.2, [M+Na]⁺ 571.2, found [M+H]⁺ 549.2, [M+Na]⁺571.2.

3. Procedure for the Preparation of 102c

A stirred mixture of 102b (160 mg, 0.30 mmol) and Cs₂CO₃ (151 mg, 0.46mmol) in DMF (15 mL) was heated to 90° C. under a N₂ atmosphere for 4 h,TLC (PE:EA=1:2) showed that the starting material was consumed. Themixture was cooled to RT, poured into ice-water (100 mL) and extractedwith EA (20 mL×2). The combined organic extracts were washed with brine(30 mL), dried over Na₂SO₄, filtered and concentrated in vacuo to give102c (100 mg, 67%) as a yellow solid. LC-MS (Agilent): R_(t) 3.94 min;ink calculated for C₃₁H₃₂N₂O₅ [M+H]⁺ 512.2, [M+Na]⁺ 535.2, found [M+H]⁺512.2, [M+Na]⁺ 535.2.

4. Procedure for the Preparation of 102

To a solution of 102c (100 mg, 0.20 mmol) in THF/water (10 mL/2 mL) wasadded LiOH.H₂O (25 mg, 0.59 mmol) and the mixture was stirred at RTovernight, TLC (DCM:MeOH=10:1) showed that the starting material wasconsumed. Most of the THF was removed in vacuo and the residue wasdissolved in water (10 mL) and washed with Et₂O. The aqueous layer wasacidified to pH 4˜5 with a 3 M aqueous HCl solution and extracted withDCM (15 mL×2). The combined organic extracts were washed with brine (15mL×2), dried over Na₂SO₄, filtered and concentrated in vacuo. Theresidue was purified by preparative HPLC to give 102 (28 mg, 29%) aswhite solid. LC-MS (Agilent): R_(t) 4.03 min; m/z calculated forC₂₉H₂₈N₄O₃ [M+H]⁺ 499.2, found [M+H]⁺ 499.2. HPLC (214 and 254 nm):R_(t) 9.14 min.

Example 42: Compound 1031-((2S,4S)-2-(hydroxymethyl)-4-(3-phenylpropoxy)-pyrrolidine-1-yl)-diphenylethanoate

To a solution of Compound 6 (400 mg, 0.9 mmol) in THF (10 mL) at −10° C.under N₂ was added BH₃.THF (1.0 M solution in THF, 1.0 mL, 1.0 mmol)dropwise and the mixture was stirred at −10° C. for 1 h, TLC(DCM:MeOH=20:1) showed there was no reaction. The reaction mixture wasallowed to warm to RT and stirred for 30 min, TLC showed most of thestarting material remained. More BH₃.THF (1.0 M solution in THF, 0.9 mL,0.9 mmol) was added and the mixture was stirred at RT overnight, TLC(DCM:MeOH=20:1) showed that most of the starting material was consumed.The mixture was cooled to 0° C., quenched with MeOH, diluted with water(20 mL) and extracted with EA (20 mL×2). The combined organic extractswere washed with a saturated aqueous NaHCO₃ solution, a 1 M aqueous HClsolution, brine and dried over Na₂SO₄, filtered and concentrated invacuo. The residue was purified by column chromatography (PE:EA=10:1 to5:1) followed by preparative HPLC to give 103 (30 mg, 7%) as a whitesolid. LC-MS (Agilent): R_(t) 4.02 min; m/z calculated for C₂₈H₃₁NO₃[M+H]⁺ 430.3, [2M+Na]⁺ 881.5, found [M+H]⁺ 430.3, [2M+Na]⁺ 881.5. HPLC(214 and 254 nm): R_(t) 9.42 min.

Example 43: Compound 104(2S,4S)-1-(2,2-diphenylacetyl)-4-(3-(4-fluorophenyl)-propoxy)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 104a

To a solution of 4-fluorocinnamic acid (2.0 g, 12 mmol) in acetone (30mL) was added Cs₂CO₃ (4.7 g, 14.4 mmol) and iodomethane (2.5 g, 18 mmol)and the mixture was stirred at RT for 3 h, TLC (PE:EA=2:1) showed thatthe starting material was consumed. The mixture was concentrated invacuo and the residue was partitioned between water (30 mL) and DCM (20mL). The organic layer was separated, washed with brine, dried overNa₂SO₄ and concentrated in vacuo to give 104a (1.9 g, 90%) as a yellowsolid. LC-MS. (Agilent): R_(t) 3.85 min; m/z calculated forC₁₀H₉FO₂[M+H]⁺ 180.1, found [M+H]⁺ 180.1.

2. Procedure for the Preparation of 1046

To a solution of 104a (1.9 g, 10.0 mmol) in DCM (20 mL) at −65° C. underN₂ was added DIBAL-H (1.2 M solution in toluene, 10.0 mL, 12.0 mmol)dropwise and the mixture was stirred at −65° C. for 1 h, TLC (PE:EA=2:1)showed incomplete reaction. More DIBAL-H (1.2 M solution in toluene, 8.3mL, 10.0 mmol) was added and stirring was continued for 30 min, TLC(PE:EA=2:1) showed that some starting material remained. More DIBAL-H(1.2 M solution in toluene, 2.5 mL, 3.0 mmol) was added and stirring wascontinued for 30 min, TLC (PE:EA=2:1) showed that the starting materialwas consumed. The mixture was allowed to warm to −10° C. and quenchedwith a 2.5 M aqueous NaOH solution (2.5 eq) then water (50 mL). DCM (30mL) was added and the resulting precipitate was removed by filtration.The filtrate was collected and the phases were separated. The aqueouslayer was extracted with DCM (30 mL) and the combined organic extractswere washed with brine, dried over Na₂SO₄, filtered and concentrated invacuo to give 104b (1.4 g, 93%) as an off-white solid.

3. Procedure for the Preparation of 104c

To a stirred suspension of 104b (0.7 g, 4.6 mmol) in THF (10 mL) wasadded PPh₃ (1.4 g, 5.5 mmol) and CBr₄ (2.3 g, 6.9 mmol) and the mixturewas stirred at RT for 1 h, TLC (PE:EA=10:1) showed that the startingmaterial was consumed. The mixture was concentrated in vacuo and theresidue was purified by column chromatography (100% PE) to give 104c(0.9 g, 90%) as a yellow oil.

4. Procedure for the Preparation of 104d

To a stirred solution of 104c (353 mg, 1.6 mmol) and 2e (380 mg, 1.1mmol) in DMF (10 mL) at −45° C. was added t-BuONa (108 m g, 1.1 mmol) inportions and the mixture was stirred at −40° C. for 1.5 h, TLC(PE:EA=1:1) showed that the starting material was consumed. The reactionwas quenched with AcOH and then allowed to warm to −10° C. Water (50 mL)was added and the mixture was extracted with EA (20 mL). The organiclayer was washed with brine, dried over Na₂SO₄, filtered andconcentrated in vacuo. The residue was purified by chromatography(PE:EA=10:1 to 5:1) to give 104d (110 mg, 21%) as a yellow oil. LC-MS(Agilent): R_(t) 4.05 min; m/z calculated for C₁₃H₁₇NO₃ [M+H]⁺ 474.2,found [M+H]⁺ 474.2.

5. Procedure for the Preparation of 104e

To a stirred solution of 104d (110 mg, 0.23 mmol) in MeOH (10 mL) wasadded 10% Pd/C (11 mg) and the mixture was stirred at RT under a H₂atmosphere (1 atm) overnight, TLC (PE:EA=2:1) showed that the startingmaterial was consumed. The mixture was filtered and the filtrate wasconcentrated in vacuo to give 104e (100 mg, 90%) as a colorless oil.

LC-MS (Agilent): R_(t) 4.08 min; m/z calculated for C₂₉H₂₈FNO₄ [M+H]⁺476.2, found [M+H]⁺ 476.2.

6. Procedure for the Preparation of 104

To a mixture of 104e (100 mg, 0.2 mmol) in THF/water (8 mL/3 mL) wasadded LiOH.H₂O (26 mg, 0.6 mmol) and the mixture was stirred at RTovernight, TLC (PE:EA=2:1) showed that the starting material wasconsumed. Most of the THF was removed in vacuo and the residue wasdissolved in water (15 mL) and washed with Et₂O (15 mL). DCM (15 mL) wasadded and the aqueous layer was acidified to pH 2-3 with a 1 M aqueousHCl solution. The layers were separated and the aqueous layer wasfurther extracted with DCM (15 mL). The combined organic layers werewashed with brine, dried over Na₂SO₄, filtered and concentrated in vacuoto give 104 (60 mg, 65%) as a white solid. LC-MS (Agilent): R_(t) 3.96min; m/z calculated for C₂₈H₂₈FNO₄ [M+H]⁺ 461.2, found [M+H]⁺ 462.2.HPLC (214 and 254 nm): R_(t) 9.34 min.

Example 44: Compound 105(2S,4S)-1-(2,2-diphenylacetyl)-4-((3-(4-methoxy-3-methylphenyl)prop-2-yn-1-yl)(methyl)amino)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 105a

A mixture of 2-(prop-2-ynyloxy)-tetrahydro-2H-pyran (1.4 g, 10.0 mmol),Cs₂CO₃ (4.8 g, 15.0 mmol), 4-bromo-1-methoxy-2-methylbenzene (2.0 g,10.0 mmol), Pd₂(dba)₃ (180 mg, 0.2 mmol) and Xantphos (100 mg, 0.17mmol) in MeCN (30 mL) was stirred at 80° C. under a N₂ atmosphereovernight. TLC (PE:EA=10:1) showed that the starting material wasconsumed. The mixture was cooled to RT, water (50 mL) was added andextracted with EA (30 mL×2). The combined organic extracts were washedwith brine, dried over Na₂SO₄, filtered and concentrated in vacuo. Theresidue was purified by column chromatography (PE:EA=1:0 to 50:1) togive 105a (450 mg, 17%) as a yellow oil. LC-MS (Agilent): R_(t) 4.49min; m/z calculated for C₁₆H₂₀O₃ [M+H]⁺ 261.1, [M+Na]⁺ 283.1, found[M+H]⁺ 261.2, [M+Na]⁺ 283.1.

2. Procedure for the Preparation of 1056

To a stirred solution of 105a (450 mg, 1.7 mmol) in MeOH (10 mL) wasadded TsOH.H₂O (5 mg, 0.03 mmol) and the mixture was stirred at RTovernight, TLC (PE:EA=2:1) showed some of the starting materialremained. More TsOH.H₂O (5 mg, 0.03 mmol) was added and stirring wascontinued at RT for 24 h, TLC showed that the starting material wasconsumed. Most of the MeOH was removed in vacuo and the residue waspartitioned between water (30 mL) and EA (20 mL). The layers wereseparated and the aqueous layer was further extracted EA (20 mL). Thecombined organic extracts were washed with brine, dried over Na₂SO₄,filtered and concentrated in vacuo to give 105b (330 mg, >100%) as ayellow oil, which was used directly in the next step. LC-MS (Agilent):R_(t) 3.56 min; m/z calculated for C₁₁H₁₂O₃₂[M+H]⁺ 177.1, [M+Na]⁺ 199.1,found [M+H]⁺ 177.1, [M+Na]⁺ 199.1.

3. Procedure for the Preparation of 105c

To a stirred suspension of 105b (320 mg, 1.8 mmol) in THF (10 mL) wasadded PPh₃ (518 mg, 1.9 mmol) and CBr₄ (782 mg, 2.4 mmol) and themixture was stirred at RT for 4 h, TLC (PE:EA=4:1) showed that thestarting material was consumed. The mixture was concentrated in vacuoand the residue was purified by column chromatography (100% PE) to give105c (400 mg, 93%) as a yellow oil.

4. Procedure for the Preparation of 105d

To a solution of 105c (350 mg, 1.0 mmol) and 105c (353 mg, 1.48 mmol) inDMF (10 mL) was added Cs₂CO₃ (480 mg, 1.48 mmol) and the mixture washeated at 60° C. for 4 h, TLC (DCM:MeOH=20:1) showed that most of 90cwas consumed. The mixture was cooled to RT, poured into ice-water (100mL) and extracted with EA (30 mL×2). The combined organic extracts werewashed with brine, dried over Na₂SO₄, filtered and concentrated invacuo. The residue was purified by column chromatography (PE:EA=5:1 to2:1) to give 105d (250 mg, 49%) as a yellow oil. LC-MS (Agilent): R_(t)4.07 min; m/z calculated for C₃₂H₃₄N₂O₄ [M+H]⁺ 511.3, found [M+H]⁺511.3.

5. Procedure for the Preparation of 105

Hydrolysis of 105d (250 mg, 0.49 mmol) was performed as described inExample 9, 3. with 3 equivalents of LiOH.H₂O (62 mg, 1.47 mmol). Afteracidification, the layers were separated and the aqueous layer wasfurther extracted with DCM (20 mL). The combined organic extracts werewashed with brine, dried over Na₂SO₄, filtered and concentrated in vacuoto give 105 (200 mg, 82%) as a yellow solid. LC-MS (Agilent): R_(t) 3.89min; m/z calculated for C₃₁H₃₂N₂O₄ [M+H]⁺ 497.2, found [M+H]⁺ 497.3.HPLC (214 and 254 nm): R_(t) 9.09 min.

Example 45: Compound 92(2S,4S)-1-(2,2-diphenylacetyl)-4-((3-(4-methoxy-3-methylphenyl)propyl)(methyl)amino)pyrrolidine-2-carboxylicacid

A mixture of Compound 105 (140 mg, 0.28 mmol) and 10% Pd/C (14 mg) in EA(10 mL) was stirred at 30° C. under a H₂ atmosphere (1 atm) overnight,LCMS analysis showed that the starting material was consumed. Themixture was filtered through Celite and the filtrate was concentrated invacuo. The residue was purified by preparative HPLC to give 92 (30 mg,21%) as a white solid. LC-MS (Agilent): R_(t) 3.84 min; m/z calculatedfor C₃₁H₃₆N₂O₄ [M+H]⁺ 501.3, found [M+H]⁺ 501.3. HPLC (214 and 254 nm):R_(t) 8.99 min.

Example 46: Compound 106(2S,4S)-1-(2,2-diphenylacetyl)-4-(4-phenylbutyl)-pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 106a

To a solution of 65a (500 mg, 2.05 mmol) in THF (5 mL) at −65° C. wasadded LiHMDS (1 M solution in THF, 2.26 mL, 2.26 mmol) and the mixturewas stirred at −65° C. for 0.5 h. A solution of PhNTf₂ (807 mg, 2.26mmol) in THF (1 mL) was then added slowly and stirring was continued at−65° C. for 3 h before allowing to warm to −30° C. and stirred for afurther 2 h. The mixture was then allowed to warm to RT and stirredovernight, TLC (PE:EA=1:1) showed that most of the starting material wasconsumed. The reaction was quenched with a saturated aqueous NaHCO₃solution and then partitioned between EA and brine. The organic layerwas separated, dried over Na₂SO₄, filtered and concentrated in vacuo.The residue was purified by chromatography (PE:EA=1:0 to 4:1) to give106a (400 mg, 52%) as a thick colorless oil.

2. Procedure for the Preparation of 106b

To a solution of 106a (250 mg, 0.66 mmol) in THF (5 mL) at RT under N₂was added 1-(but-3-ynyl)benzene (104 mg, 0.80 mmol), DIPEA (425 mg, 3.30mmol), CuI (13 mg, 0.068 mmol) and Pd(PPh)₂Cl₂ (21 mg, 0.033 mmol) andthe mixture was stirred at RT for 3 h, TLC (PE:EA=10:1) showed that thestarting material was consumed. The mixture was partitioned betweenbrine (20 mL) and EA (20 mL) and the organic layer was separated, driedover Na₂SO₄, filtered and concentrated in vacuo. The residue waspurified by chromatography (PE:EA=1:0 to 20:1) to give 106b (120 mg,51%) as a yellow oil and an impure fraction of 106b (40 mg). LC-MS(Agilent). R_(t) 4.42 min; m/z calculated for C₂₁H₂₅NO₄[M+Na]⁺ 378.2,[M-t-Bu]⁺ 300.1, found [M+Na]⁺ 378.2, [M-t-Bu]⁺ 300.1.

3. Procedure for the Preparation of 106c

To a solution of 106b (170 mg, 0.48 mmol) in MeOH (5 mL) was added 10%Pd/C (20 mg) and the mixture was stirred under a H₂ atmosphere (1 atm)at RT overnight, TLC (PE:EA=10:1) showed that the starting material wasconsumed. The mixture was filtered and the filtrate was concentrated invacuo to give 106c (160 mg, 94%) as colorless oil. LC-MS (Agilent):R_(t) 4.48 min; m/z calculated for C₂₁H₃₁NO₄ [M+Na]⁺ 384.2, [M-t-Bu]⁺306.2, [M-boc]⁺ 262.2, found [M+Na]⁺ 384.2, [M-t-Bu]⁺ 306.2, [M-boc]⁺262.2.

4. Procedure for the Preparation of 106d

A solution of 106c (160 mg, 0.44 mmol) in a 4 M HCl/MeOH solution (5 mL)was stirred at RT for 3 h, TLC (PE:EA=4:1) showed that the startingmaterial was consumed. The mixture was concentrated in vacuo, theresidue was dissolved in water (15 mL), basified to pH 7-8 with K₂CO₃and extracted with DCM (15 mL×3). The combined organic extracts werewashed with brine (15 mL), dried over Na₂SO₄, filtered and concentratedin vacuo to give the product (90 mg) as a yellow oil. NMR analysisrevealed the cis/trans ratio to be 6.1:1. To a solution of thedeprotected amine (90 mg) in DCM (10 mL) was added diphenyl acetic acid(90 mg, 0.44 mmol) and EDCI.HCl (95 mg, 0.49 mmol) and the mixture wasstirred at RT overnight, TLC (DCM:MeOH=10:1) showed that the startingmaterial was consumed. The mixture was washed with brine, dried overNa₂SO₄, filtered and concentrated in vacuo. The residue was purified bychromatography (PE:EA=1:0 to 4:1) to give 106d (120 mg, 59%) as acolorless oil. LC-MS (Agilent): R_(t) 4.54 min; m/z calculated forC₃₀H₃₃NO₃[M+H]⁺ 455.2, found [M+H]⁺ 455.2.

5. Procedure for the Preparation of Compound 106

Hydrolysis of 106d (120 mg, 0.26 mmol) was performed as described inExample 53, 2. with about 3 equivalents of LiOH.H₂O (33 mg, 0.79 mmol).The combined organic extracts were washed with brine (10 mL×2), driedover Na₂SO₄, filtered and concentrated in vacuo to give 106 (110 mg,94%) as a colorless gum. LC-MS (Agilent): R_(t) 4.55 min; m/z calculatedfor C₂₉H₃₁NO₃ [M+H]⁺ 442.2, found [M+H]⁺ 442.2. HPLC (214 and 254 nm):R_(t) 9.62 min.

Example 47: Compound 139(S)-1-(2,2-diphenylacetyl)-4-(3-phenylthiophen-2-yl)-2,5-dihydro-1H-pyrrole-2-carboxylicacid

1. Procedure for the Preparation of 139a

To a solution of 3-bromo thiophene (15.0 g, 92 mmol) and phenyl boronicacid (16.8 g, 138 mmol) in DME (150 mL) was added Pd(PPh₃)₄, (1.0 g,0.87 mmol) and the mixture was heated at reflux overnight under a N₂atmosphere, TLC (PE) showed most of the starting material was consumed.The mixture was cooled to RT, washed with brine (100 mL), dried overNa₂SO₄, filtered and concentrated in vacuo. The residue was purified bycolumn chromatography (PE) to give 139a (4.0 g, 27%) as light yellowsolid, which was used directly in the next step.

2. Procedure for the Preparation of 139b

To a stirred solution of 139a (2.0 g, 12.5 mmol) in DMF (40 mL) at 0° C.under N₂ was added a solution of NBS (2.43 g, 13.7 mmol) in DMF (20 mL)dropwise and the mixture was stirred at RT overnight, TLC analysis(hexane) showed that the starting material was consumed. The mixture waspoured into water (300 mL), extracted with EA (50 mL×2) and the combinedorganic extracts were washed with water (40 mL), brine, dried overNa₂SO₄, filtered and concentrated in vacuo to give 139b (3.0 g, 100%) asa yellow oil.

3. Procedure for the Preparation of 139c

To a stirred solution of 139b (1.0 g, 4.2 mmol) in THF (20 mL) at −70°C., under N₂ was added t-BuLi (1.3 M solution in hexane, 3.5 mL, 4.6mmol) dropwise and the mixture was stirred at −70° C. for 2 h.2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (950 mg, 5.1 mmol)was added dropwise and stirring was continued at −70° C. for a further 3h. The mixture was allowed to warm to RT and stirred for a further 1 h,TLC (PE) showed that the starting material was consumed. The mixture wascooled to 0° C., water was added (30 mL) and extracted with EA (20mL×2). The combined organic extracts were washed with brine, dried overNa₂SO₄, filtered and concentrated in vacuo. The residue was purified bycolumn chromatography (PE:EA=1:0 to 50:1) to give 139c (700 mg, 58%) asyellow solid. LC-MS (Agilent): R_(t) 4.64 min; m/z calculated forC₁₆H₁₉BO₂S [M+H]⁺ 287.1, [M+Na]⁺ 309.1, found [M+H]⁺ 287.1, [M+Na]⁺309.1.

4. Procedure for the Preparation of 139d

To a mixture of 139c (515 mg, 1.8 mmol) and 106a (675 mg. 1.8 mmol) intoluene (10 mL) was added a 2 M aqueous Na₂CO₃ solution (2.7 mL, 5.4mmol) and Pd(PPh₃)₄ (104 mg, 0.09 mmol, 5 mol %) and the mixture washeated at 105° C. overnight under a N₂ atmosphere, TLC (PE:EA=10:1)showed that most of the starting materials were consumed. The mixturewas cooled to RT, diluted with water (20 mL) and extracted with EA (15mL×2). The combined organic extracts were washed with brine,concentrated in vacuo and the residue was purified by columnchromatography (PE to PE:EA=40:1) to give 139d (600 mg, 86%) as yellowoil. LC-MS (Agilent): R_(t) 4.60 min; m/z calculated for C₂₁H₂₃NO₄S[M−100]⁺ 286.1, [M+Na]⁺ 408.1, [M−56]⁺ 330.1, found [M−100]⁺ 286.1,[M+Na]⁺ 408.1, [M−56]⁺ 330.1.

5. Procedure for the Preparation of 139e

139d (600 mg, 1.56 mmol) was dissolved in a 4 M HCl/MeOH solution (15mL) and the mixture was stirred at RT overnight, TLC (PE:EA=2:1) showedthat the starting material was consumed. Most of the MeOH was removed invacuo and the residue was diluted with water (20 mL) and washed withEt₂O (15 mL×2). The aqueous layer was basified to pH 8 with a saturatedaqueous Na₂CO₃ solution and extracted with DCM (15 mL×2). The combinedorganic extracts were washed with brine, dried over Na₂SO₄, filtered andconcentrated in vacuo and the residue was purified by columnchromatography (PE:EA=15:1 to 5:1) to give 139e (170 mg, 38%) as ayellow oil. LC-MS (Agilent): R_(t) 3.51 min; m/z calculated forC₁₇H₁₇NO₂S [M+H]⁺ 286.1, found [M+H]⁺ 286.1.

6. Procedure for the Preparation of 139f.

To a solution of 139e (160 mg, 0.56 mmol) and Et₃N (85 mg, 0.84 mmol) inDCM (5 mL) at 0° C. was added a solution of diphenylacetyl chloride (155mg, 0.67 mmol) in DCM (2 mL) and the mixture was stirred at RT for 15min, TLC (PE:EA=4:1) showed that the starting material was consumed. Themixture was washed with brine, dried over Na₂SO₄, filtered andconcentrated in vacuo. The residue was purified by column chromatography(PE:EA=15:1 to 8:1) to give 139f (130 mg, 48%) as a yellow solid. LC-MS(Agilent): R_(t) 4.37 min; m/z calculated for C₃₀H₂₅NO₃S [M+H]⁺ 480.2,found [M+H]⁺ 480.2.

7. Procedure for the Preparation of 139

To a mixture of 139f (130 mg, 0.27 mmol) in THF/water (6 mL/2 mL) wasadded LiOH.H₂O (23 mg, 0.54 mmol) and the mixture was stirred at RTovernight, TLC (PE:EA=2:1) showed showed that the starting material wasconsumed. Most of the THF was removed in vacuo and the residue waspartitioned between water (15 mL) and DCM (15 mL) and the aqueous phasewas acidified to pH 2-3 with a 1 M aqueous HCl solution. The layers wereseparated and the aqueous phase was extracted with DCM (15 mL). Thecombined organic extracts were washed with brine, dried over Na₂SO₄,filtered and concentrated in vacuo to give 139 (100 mg, 80%) as whitesolid. LC-MS (Agilent): R_(t) 4.43 min; m/z calculated for C₂₉H₂₃NO₃S[M+H]⁺ 466.1 found [M+H]⁺ 466.1. HPLC (JULY-L) (214 and 254 nm): R_(t)9.46 min.

Example 48: Compound 107(2S,4S)-1-(2,2-diphenylacetyl)-4-(3-phenylthiophen-2-yl)-pyrrolidine-2-carboxylicacid

A mixture of 139 (60 mg, 0.13 mmol) and 10% Pd/C (6 mg) in MeOH (10 mL)was stirred at RT under a H₂ atmosphere (1 atm) overnight, TLC(DCM:MeOH=10:1) showed that the starting material was consumed. Themixture was filtered and the filtrate was concentrated in vacuo. Theresidue was purified by preparative HPLC to give 107 (15 mg, 25%) aswhite solid. LC-MS (Agilent): R_(t) 4.51 min; m/z calculated forC₂₉H₂₅NO₃S [M+H]⁺ 468.1 found [M+H]⁺ 468.1. HPLC (JULY-L) (214 and 254nm): R_(t) 9.44 min.

Example 49: Compound 140(S)-1-(2,2-diphenylacetyl)-4-(4-phenylbut-1-yn-1-yl)-2,5-dihydro-1H-pyrrole-2-carboxylicacid

1. Procedure for the Preparation of 140a

106b (40 mg, 0.089 mmol) was dissolved in a 4 M HCl/MeOH solution (5 mL)at RT and the mixture was stirred for 4 h, TLC (PE:EA=4:1) showed thatthe starting material was consumed. The mixture was concentrated invacuo and the residue was dissolved in water (20 mL) and washed withether (15 mL). DCM (15 mL) was added and the aqueous layer was basifiedto pH 8 with a saturated aqueous NaHCO₃ solution. The layers wereseparated and the aqueous phase was extracted with DCM (15 mL). Thecombined organic extracts were washed with brine, dried over Na₂SO₄,filtered and concentrated in vacuo to give 140a (30 mg, 98%) as a yellowoil. LC-MS (Agilent): R_(t) 3.55 min; m/z calculated for C₁₆H₁₇NO₂[M+H]⁺256.04, found [M+H]⁺ 256.1.

2. Procedure for the Preparation of 140b

To solution of 140a (30 mg, 0.11 mmol) and diphenylacetic acid (25 mg,0.11 mmol) in DCM (5 mL) at RT was added EDCI.HCl (32 mg, 0.16 mmol) andthe mixture was stirred overnight, TLC (PE:EA=2:1) showed that most ofthe starting material was consumed. The mixture was washed with brine,dried over Na₂SO₄, filtered and concentrated in vacuo. The residue waspurified by chromatography (PE:EA=1:0 to 4:1) to give 140b (40 mg, 81%)as a yellow solid. LC-MS (Agilent): R_(t) 4.52 min; m/z calculated forC₃₀H₂₇NO₃ [M+H]⁺ 450.2, found [M+H]⁺ 450.2.

3. Procedure for the Preparation of 140

Hydrolysis of 140b (40 mg, 0.089 mmol) was performed as described inExample 9, 3. with about 2 equivalents of LiOH.H₂O (7 mg, 0.18 mmol).After acidification, the layers were separated and the aqueous phase wasextracted with DCM (10 mL). The combined organic extracts were washedwith brine, dried over Na₂SO₄, filtered and concentrated in vacuo. Theresidue was purified by preparative HPLC to give 140 (10 mg, 26%) as awhite solid. LC-MS (Agilent): R_(t) 3.95 min; m/z calculated forC₂₉H₂₅NO₃ [M+H]⁺ 436.2, found [M+H]⁺ 436.2. HPLC (214 and 254 nm): R_(t)9.49 min.

Example 50: Compound 112(2S,4S)—N—(N,N-dimethylsulfamoyl)-1-(2,2-diphenylacetyl)-4-(3-phenylpropoxy)pyrrolidine-2-carboxamide

To a solution of Compound 6 (50 mg, 0.11 mmol) and N,N-dimethylsulfamide(15 mg, 0.12 mmol) in DCM (1 mL) was added DCC (27 mg, 0.13 mmol) andthe mixture was stirred in a sealed flask at RT overnight, LCMS analysisshowed that the starting material was consumed. DCM (5 mL) and PE (3 mL)were added to the mixture and the white solid was removed by filtration.The filtrate was concentrated in vacuo and the residue was purified bypreparative HPLC to give 112 (15 mg, 25%) as a white solid. LC-MS(Agilent): R_(t) 3.25 min; m/z calculated for C₃₀H₃₅N₃O₅S [M+H]⁺ 550.2,found [M+H]⁺ 550.3. HPLC (JULY-L) (214 and 254 nm): R_(t) 9.27 min.

Example 51: Compound 115(2S,4S)-4-(6-benzyl-7-oxa-2,6-diazaspiro[4,5]decan-2-yl)-1-(2,2-diphenylacetyl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 115a

To a solution of 61a (142 mg, 0.42 mmol) and6-benzyl-8-oxa-2,6-diazaspiro[4.5]decan-7-one hydrochloride (100 mg,0.42 mmol) in MeOH (10 mL) was added Et₃N (43 mg, 0.42 mmol) followed by2 drops of AcOH and the mixture was stirred at RT for 1 h. NaCNBH₃ (40mg, 0.63 mmol) was added and stirring was continued at RT overnight, TLC(DCM:MeOH=10:1) showed that the starting material was consumed. Themixture was concentrated in vacuo and the residue was purified by columnchromatography (DCM:MeOH=100:1 to 50:1) to give 115a (100 mg, 42%) as alight yellow solid. LC-MS (Agilent): R_(t) 3.96 min; m/z calculated forC₃₄H₃₇N₃O₅ [M+H]⁺ 568.3, found [M+H]⁺ 568.3.

2. Procedure for the Preparation of 115

Hydrolysis of 115a (20 mg, 0.035 mmol) was performed as described inExample 9, 3. with 2 equivalents of LiOH.H₂O (3 mg, 0.07 mmol). Theorganic layer was separated, washed with brine, dried over Na₂SO₄,filtered and concentrated in vacuo. The residue was purified bypreparative HPLC to give 115 (10 mg, 50%) as a white solid. LC-MS(Agilent): R_(t) 3.94 min; m/z calculated for C₃₃H₃₅N₃O₅ [M+H]⁺ 554.3found [M+H]⁺ 554.3. HPLC (JULY-L) (214 and 254 nm): R_(t) 8.77 min.

Example 52: Compound 116(2S,4S)1-(2,2-diphenylacetyl)-4-(methyl(3-phenylprop-2-yn-1-yl)amino)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 116a

To a solution of 3-phenylprop-2-yn-1-ol (930 mg, 7.04 mmol) and PPh₃(1.85 g, 7.04 mmol) in THF (20 mL) was added CBr₄ (2.10 g, 6.33 mmol)portion-wise and the mixture was stirred at RT overnight, TLC (100% PE)showed that most of the starting material was consumed. PE (15 mL) wasadded and the resulting precipitate was removed by filtration. Thefiltrate was concentrated in vacuo and the residue was purified bychromatography (100% PE) to give 116a (1.10 g, 81%) as a colorless oil.

2. Procedure for the Preparation of 116b

A mixture of 90c (80 mg, 0.23 mmol), 116a (53 mg, 0.27 mmol) and Cs₂CO₃(89 mg, 0.27 mmol) in DMF (8 mL) was heated at 60° C. overnight, TLC(DCM:MeOH=20:1) showed that most of the starting material was consumed.The mixture was poured into ice-water (40 mL), extracted with EA (20mL×2) and the combined organic extracts were washed with brine (15 mL),dried over Na₂SO₄, filtered and concentrated in vacuo. The residue waspurified by chromatography (PE:EA=1:0 to 2:1) to give 116b (60 mg, 57%)as thick colorless oil. LC-MS (Agilent): R_(t) 4.24 min; m/z calculatedfor C₃₀H₃₀N₂O₃ [M+H]⁺ 467.2, found [M+H]⁺ 467.2.

3. Procedure for the Preparation of 116

A mixture of 116b (60 mg, 0.13 mmol) and LiOH.H₂O (16 mg, 0.39 mmol) inTHF/water (8 mL/2 mL) was stirred at RT overnight, TLC (PE:EA=1:1)showed that the starting material was consumed. Most of the THF wasremoved in vacuo, the residue was dissolved in water (8 mL) and washedwith MTBE (6 mL×2). The aqueous layer was then acidified to pH 4˜5 witha 4 M aqueous HCl solution. The resulting precipitate was collected byfiltration and purified by preparative HPLC to give 116 (32 mg, 55%) asa white solid. LC-MS (Agilent): R_(t) 3.81 min; m/z calculated forC₂₉H₂₈N₂O₃ [M+H]⁺ 453.2, found [M+H]⁺ 453.2. HPLC (JULY-L) (214 and 254nm): R_(t) 8.91 min.

Example 53: Compound 124(2S,4S)-1-(2,2-diphenylacetyl)-4-((3-phenylpropyl)thio)-pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 124a

To a solution of PhCOSH (1.42 g, 9.60 mmol) in DMF (70 mL) at 0° C.under N₂ was added NaH (0.39 g, 9.60 mmol) slowly and the mixture wasstirred at RT for 30 min. 17a (2.00 g, 4.8 mmol) was then added and themixture was stirred at RT overnight, TLC (PE:EA=1:1) showed that thestarting material was consumed. The mixture was poured into water,extracted with EA and the organic extract was washed with a saturatedaqueous NaHCO₃ solution, brine, dried over Na₂SO₄, filtered andconcentrated in vacuo. The residue was purified by chromatography(PE:EA=1:0 to 5:1) to give 124a (1.61 g, 73%) as a yellow solid. LC-MS(Agilent, P-2): R_(t) 3.14 min; m/z calculated for C₂₋₄H₂₅NO₄S [M+H]⁺460.1, [M+Na]⁺ 482.1, found [M+H]⁺ 460.1, [M+Na]⁺ 482.1.

2. Procedure for the Preparation of 124b

A mixture of 124a (1.61 g, 3.50 mmol) and K₂CO₃ (968 mg, 7.01 mmol) inMeOH (20 mL) was stirred at RT for 20 min, TLC (PE:EA=2:1) showed thatthe starting material was consumed. Most of the MeOH was removed invacuo and the residue was diluted with brine (30 mL) and extracted withEA (30 mL×2). The combined organic extracts were dried over Na₂SO₄,filtered and concentrated in vacuo to give crude 124b (1.58 g) as thickyellow oil, which was used directly in the next step withoutpurification. LC-MS (Agilent, P-2): R_(t) 2.93 min; in/z calculated forC₂₀H₂₁NO₃S [M+H]⁺ 356.1, [M+Na]⁺ 378.1, found [M+H]⁺ 356.1, [M+Na]⁺378.1.

3. Procedure for the Preparation of 124c

To a stirred mixture of 124b (600 mg, 1.69 mmol) and K₂CO₃ (257 mg, 1.86mmol) in DMF (20 mL) was added 1-bromo-3-phenylpropane (370 mg, 1.86mmol) and the mixture was heated at 80° C. overnight, TLC (PE:EA=2:1)showed that the starting material was consumed. The mixture was pouredinto ice-water (100 mL) and EA (40 mL). The organic layer was separated,washed with brine (30 mL×2), dried over Na₂SO₄, filtered andconcentrated in vacuo. The residue was purified by chromatography(PE:EA=1:0 to 4:1) to give 124c (448 mg, 71%) as a colorless oil. LC-MS(Agilent, P-2): R_(t) 3.26 min; m/z calculated for C₂₉H₃₁NO₃S [M+H]⁺472.2, [M+Na]⁺ 496.2, found [M+H]⁺ 472.2, [M+Na]⁺ 496.2.

4. Procedure for the Preparation of 124

A mixture of 124c (146 mg, 0.31 mmol) and LiOH.H₂O (39 mg, 0.93 mmol) inTHF/water (8 mL/2 mL) was stirred at RT overnight, TLC (PE:EA=2:1)showed that the starting material was consumed. Most of the THF wasremoved in vacuo, the residue was dissolved in water (10 mL), acidifiedto pH 4˜5 with a 4 M aqueous HCl solution and extracted with DCM (15mL×2). The combined organic extracts were washed with brine (10 mL×2),dried over Na₂SO₄, filtered and concentrated in vacuo. The residue waspurified by chromatography (PE:EA=4:0 to 2:1) to give 124 (97 mg, 68%)as a colorless oil. LC-MS (Agilent, P-2): R_(t) 2.87 min; m/z calculatedfor C₂₈H₂₉NO₃S [M+H]⁺ 460.2, [M+Na]⁺ 482.2, found [M+H]⁺ 460.2, [M+Na]⁺482.2. HPLC (JULY-L) (214 and 254 nm): R_(t) 9.41 min

Example 54: Compound 125(2S,4S)-1-(2,2-diphenylacetyl)-4-((3-phenylpropyl)-sulfonyl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 125a.

To a solution of 124c (260 mg, 0.55 mmol) in DCM (15 mL) was added 80%m-CPBA (296 mg, 1.37 mmol) and the mixture was stirred at RT overnight,TLC (PE:EA=2:1) showed that the starting material was consumed. Themixture was washed with a saturated aqueous Na₂CO₃ solution (15 mL),brine (15 mL×2), dried over Na₂SO₄, filtered and concentrated in vacuo.The residue was purified by chromatography (PE:EA=8:1 to 2:1) to give125a (245 mg, 88%) as a thick colorless oil. LC-MS (Agilent, P-2): R_(t)3.03 min; m/z calculated for C₂₉H₃₁NO₅S [M+H]⁺ 506.2, [M+Na]⁺ 528.2,found [M+H]⁺ 506.2, [M+Na]⁺ 528.2.

2. Procedure for the Preparation of 125

Hydrolysis of 125a (245 mg, 0.48 mmol) was performed as described inExample 53, 2. with about 3 equivalents of LiOH.H₂O (61 mg, 1.45 mmol).The organic extract was washed with brine (15 mL×2), dried over Na₂SO₄,filtered and concentrated in vacuo to give 125 (215 mg, 90%) as a whitesolid. LC-MS (Agilent, P-2): R_(t) 2.73 min; m/z calculated forC₂₈H₂₉NO₅S [M+H]⁺ 492.2, [M+Na]⁺ 514.2, found [M+H]⁺ 492.2, [M+Na]⁺514.2. HPLC (JULY-L) (214 and 254 nm): R_(t) 8.95 min.

Example 55: Compound 142(2S,3S)-1-(2,2-diphenylacetyl)-3-(3-phenylpropoxy)-azetidine-2-carboxylicacid and(2R,3R)-1-(2,2-diphenylacetyl)-3-(3-phenylpropoxy)-azetidine-2-carboxylicacid

1. Procedure for the Preparation of 142b

To a mixture of 142a (300 mg, 0.69 mmol) in DCE (10 mL) was addedtert-butyl 2,2,2-trichloroacetimidate (168 mg, 0.77 mmol) and themixture was heated at 60° C. overnight, TLC(DCM:MeOH=10:1) showed thatthe starting material was consumed. The mixture was washed with brine(10 mL), dried over Na₂SO₄, filtered and concentrated in vacuo. Theresidue was purified by chromatography (PE:EA=1:0 to 4:1) to give 142b(270 mg, 81%) as a white solid. LC-MS (Agilent): R_(t) 4.81 min; m/zcalculated for C₃₁H₃₅NO₄ [M+H]⁺ 486.3, [M-t-Bu]⁺ 430.2, found [M+H]⁺486.3, [M-t-Bu]⁺ 430.2.

2. Procedure for the Preparation of 142c

To a stirred solution of 142b (170 mg, 0.35 mmol) in THF (10 mL) at −65°C. under N₂ was added LDA (1 M in THF, 0.7 mL, 0.70 mmol) and themixture was allowed to warm slowly to RT and stirred overnight. Themixture was cooled in an ice-water bath and the reaction was quenchedwith a saturated aqueous NH₄Cl solution. The mixture was partitionedbetween EA (20 mL) and brine (30 mL), the organic layer was separated,dried over Na₂SO₄, filtered and concentrated in vacuo. The residue waspurified by chromatography (PE:EA=1:0 to 10:1) to give the trans-product(70 mg, 41%) as a colorless oil and the cis starting material (50 mg,29%) as a white solid. LC-MS (Agilent): R₁ 4.47 min; m/z calculated forC₃₁H₃₅NO₄ [M+H]⁺ 486.3, [M-t-Bu]⁺ 430.2, found [M+H]⁺ 486.3, [M-t-Bu]⁺430.2.

3. Procedure for the Preparation of 142

To a stirred mixture of 142c (70 mg, 0.14 mmol) in THF/water (3 mL/1 mL)was added LiOH.H₂O (18 mg, 0.43 mmol) and the mixture was stirred at RTovernight, TLC (PE:EA=4:1) showed that the starting material wasconsumed. Most of the THF was removed in vacuo, the residue wasdissolved in water (15 mL) and acidified to pH 3-4 with a 3 M aqueousHCl solution. The aqueous mixture was extracted with DCM (15 mL×2) andthe combined organic extracts were washed with brine, dried over Na₂SO₄,filtered and concentrated in vacuo to give 142 (60 mg, 92%) as a whitesolid. LC-MS (Agilent): R_(t) 4.36 min; m/z calculated for C₂₇H₂₇NO₄[M+H]⁺ 430.2, found [M+H]⁺ 430.2. HPLC (JULY-L) (214 and 254 nm): R_(t)9.33 min.

Example 56: Compound 1081-((2R,3S)-2-(hydroxymethyl)-3-(3-phenylpropoxy)-azetidin-1-yl)-2,2-diphenylethanoneand14(2S,3R)-2-(hydroxymethyl)-3-(3-phenylpropoxy)-azetidin-1-yl)-2,2-diphenylethanone

To a solution of 142 (30 mg, 0.07 mmol) in dry THF (10 mL) at 0° C.under N₂ was added Et₃N (7 mg, 0.07 mmol) followed by ClCO₂Et (7.6 mg,0.07 mmol) and the mixture was stirred at 0° C. for 1 h. NaBH₄ (8 mg,0.21 mmol) was added and stirring was continued at 0° C. for 1 h beforeallowing to warm slowly to RT and stirred overnight, TLC (PE:EA=2:1)showed that the starting material was consumed. The reaction wasquenched with water (30 mL) and the mixture was extracted with EA (15mL×2). The combined organic extracts were washed with brine, dried overNa₂SO₄, filtered and concentrated in vacuo. The residue was purified bypreparative HPLC to give 108 (15 mg, 51%) as a colorless oil.

LC-MS (Agilent): R_(t) 4.34 min; m/z calculated for C₂₇H₂₉NO₃ [M+H]⁺416.2, found [M+H]⁺ 416.2. HPLC (JULY-L) (214 and 254 nm): R_(t) 9.32min.

Example 57: Compound 109(1-((2R,3R)-2-(hydroxymethyl)-3-(3-phenylpropoxy)-azetidin-1-yl)-2,2-diphenylethanoneand(1-((2S,3S)-2-(hydroxymethyl)-3-(3-phenylpropoxy)-azetidin-1-yl)-2,2-diphenylethanone

1. Procedure for the Preparation of 109a

To a solution of 3-phenylpropan-1-ol (54.0 g, 0.40 mol) in DMF (250 mL)at RT was added NaH (60% dispersion in oil, 15.6 g, 0.40 mol) and themixture was stirred at RT for 1 h, then heated at 61° C. for 1 h. Themixture was cooled to 5° C. and 2-chloroacetic acid (15.0 g, 0.16 mol)was added. The mixture was stirred at RT for 0.5 h, then heated at 60°C. for 3 h, TLC (DCM:MeOH=10:1) showed that a new product was formed.The mixture was allowed to cool to RT, stirred overnight then pouredinto ice-water (1.5 L) and washed with EA (300 mL×4). The aqueous layerwas acidified to pH 5 with a 3 M aqueous HCl solution and extracted withEA (500 mL×2). The combined organic extracts were washed with brine (300mL×2), dried over Na₂SO₄, filtered and concentrated in vacuo to give109a (25 g, 81%) as a pale yellow solid. LC-MS (Agilent): R_(t) 3.74min; m/z calculated for C₁₁H₁₄O₃ [M+Na]⁺ 217.1, found [M+Na]⁺ 217.1.

2. Procedure for the Preparation of 1096

To a solution of 109a (17.1 g, 87.9 mmol) in DCM (150 mL) was addedSOCl₂ (11.0 g, 92.3 mmol) and the mixture was heated at reflux for 0.5h, then cooled to RT and concentrated in vacuo to give the acid chloridewhich was used directly in the next step. To a solution of ethylglyoxylate (6.00 g, 50% toluene solution, 29.3 mmol) in toluene (60 mL)was added benzyl amine (3.15 g, 29.3 mmol) and the mixture was stirredat RT for 1 h. Triethylamine (10.4 g, 103 mmol) was added and themixture was cooled in an ice-water bath. A solution of theabove-prepared acid chloride in toluene (45 mL) was then added dropwiseand the mixture was stirred at RT overnight, TLC (PE:EA=4:1) showed thatthe product was formed. The mixture was partitioned between EA (60 mL)and brine (100 mL). The organic layer was separated and washed withbrine (100 mL), dried over Na₂SO₄, filtered and concentrated in vacuo.The residue was purified by chromatography (PE:EA=1:0 to 10:1) to give109b (1.2 g, 11%) as a colorless oil. LC-MS (Agilent): R_(t) 4.15 min;m/z calculated for C₂₂H₂₅NO₄ [M+H]⁺ 368.2, [M+Na]⁺ 390.2, found [M+H]⁺368.2, [M+Na]⁺ 390.2.

3. Procedure for the Preparation of 109c

To a mixture of AlCl₃ (333 mg, 2.49 mmol) in dry THF (5 mL) at 0° C.under N₂ was added LiAlH₄ (95 mg, 2.49 mmol) and the mixture was heatedat 35° C. for 0.5 h then re-cooled to 0° C. A solution of 109b (200 mg,0.54 mmol) in THF (2 mL) was then added and the mixture was heated at35° C. for 3 h, TLC (PE:EA=2:1) showed that the starting material wasconsumed. The mixture was cooled to 0° C., the reaction was quenchedwater (1 mL) and then partitioned between EA and brine. The organiclayer was separated, dried over Na₂SO₄, filtered and concentrated invacuo to give 109c (160 mg, 95%) as a yellow oil. LC-MS (Agilent): R_(t)3.37 min; m/z calculated for C₂₀H₂₅NO₂ [M+H]⁺ 312.2, found [M+H]⁺ 312.2.

4. Procedure for the Preparation of 109d

A mixture of 109c (160 mg, 0.51 mmol) and 10% Pd/C (20 mg) in MeOH (5mL) was stirred at RT under a H₂ atmosphere (1 atm) at 35*C overnight,TLC (DCM:MeOH=10:1) showed that the starting material was consumed. Themixture was filtered and the filtrate was concentrated in vacuo to give109d (100 mg, 87%) as a colorless oil. LC-MS (Agilent): R_(t) 3.53 min;m/z calculated for C₁₃H₁₉NO₂ [M+H]⁺ 222.1, found [M+H]⁺ 222.1.

5. Procedure for the Preparation of 109

To a solution of 109d (100 mg, 0.45 mmol) and Et₃N (50 mg, 0.49 mmol) inDCM (10 mL) at 0° C. was added a solution of diphenylacetyl chloride(104 mg, 0.45 mmol) in DCM (1 mL) and the mixture was stirred at 0° C.for 1 h, TLC (DCM:MeOH=10:1) showed that the starting material wasconsumed. The mixture was washed with brine, dried over Na₂SO₄, filteredand concentrated in vacuo. The residue was purified by chromatography(PE:EA=1:0 to 4:1) to give 109 (80 mg, 43%) as a colorless oil. LC-MS(Agilent): R_(t) 3.80 min; in/z calculated for C₂₇H₂₉NO₃ [M+H]⁺ 416.2,found [M+H]⁺ 416.2. HPLC (214 and 254 nm): R_(t) 9.36 min.

Example 58: Compound 143(2R,3R)-3-(3-phenylpropoxy)-1-(2,2-diphenylacetyl)-azetidine-2-carboxylicacid and(2S,3S)-3-(3-phenylpropoxy)-1-(2,2-diphenylacetyl)-azetidine-2-carboxylicacid

To a stirred solution of 109 (250 mg, 0.60 mmol) in acetone (5 mL) at 0°C. was added Jone's reagent (0.92 mL, 2.40 mmol) and the mixture wasstirred at 0° C. for 2 h, TLC (PE:EA=2:1) showed that the startingmaterial was consumed. The reaction was quenched with iso-propanol (1mL) then diluted with EA (20 mL) and filtered. The filtrate wasconcentrated in vacuo and the residue was dissolved in EA (20 mL),washed with water (15 mL×2), saturated aqueous EDTA solution (10 mL×2),brine (15 mL×2), then dried over Na₂SO₄, filtered and concentrated invacuo to give crude 143t (240 mg) as a brown oil. A portion (40 mg) ofthe crude product was purified by preparative TLC (DCM:MeOH=10:1) togive pure 143 (20 mg) as a white solid. LC-MS (Agilent): R_(t) 4.27 min;m/z calculated for C₂₇H₂₇NO₄ [M+H]⁺ 430.2, found [M+H]⁺ 430.2. HPLC (214and 254 nm): R_(t) 9.24 min.

Example 59: Compound 54(2S,4S)-4-((benzyloxymethyl)-1-(2,2-diphenylacetyl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 54a

To a stirred solution of trans-4-hydroxy-L-proline (100 g, 0.76 mol) inEtOH (1 L) was added SOCl₂ (95.2 g, 0.8 mol) dropwise and the mixturewas heated at reflux overnight. The mixture was cooled to RT andconcentrated in vacuo to give 54a (140 g, 94%) as a white solid. LC-MS(Agilent): R_(t) 0.56 min; m/z calculated for C₁₃H₁₇NO₃ [m+H]⁺ 160.1,found [M+H]⁺ 160.1.

2. Procedure for the Preparation of 54b

To a stirred mixture 54a (60.0 g, 0.30 mol) in diethyl ether/H₂O (100mL/600 mL) at 0° C. was added K₂CO₃ (104 g, 0.75 mol) and CbzCl (48.0 g,0.28 mol) dropwise and the mixture was stirred at RT for 2 h, TLC(PE:EA=2:1) showed that a major new product was formed. The layers wereseparated and the aqueous phase was extracted with EA (100 mL×2) and thecombined organic extracts were washed with brine, dried over Na₂SO₄,filtered and concentrated in vacuo to give 54b (75.0 g, 83%) as a yellowoil. LC-MS (Agilen, P-2): R_(t) 2.86 min; m/z calculated for C₁₅H₁₉NO₅[M+H]⁺ 294.1, [M+Na]⁺ 316.1 found [M+H]⁺ 294.1, [M+Na]⁺ 316.1.

3. Procedure for the Preparation of 54c

To a stirred solution of 54b (145 g, 0.49 mol) and Et₃N (60.05 g, 0.59mol) in DCM (1 L) at RT was added TsCl (104 g, 0.54 mol) in portionsover 20 min and the mixture was heated at 40° C. overnight, TLC(PE:EA=2:1) showed that the starting material was consumed. The mixturewas cooled to RT, washed with water (200 mL×2), brine (200 mL×2), driedover Na₂SO₄, filtered and concentrated in vacuo. The residue waspurified by chromatography (PE:EA=20:1 to 1:1) to give 54c (128 g, 58%)as a yellow oil. LC-MS (Agilent, P-2): R_(t) 3.025 min; m/z calculatedfor C₂₂H₂₅NO₇S [M+H]⁺ 448.1, [M+Na]⁺ 470.1, found [M+H]⁺ 448.2, [M+Na]⁺470.1.

4. Procedure for the Preparation of 54d

A mixture 54c (34.4 g, 76.8 mmol), CsF (58.4 g, 384 mmol) and TMSCN(38.1 g, 384 mmol) in DMF (300 mL) was heated at 60° C. for 40 h, TLC(PE:EA=2:1) showed about half of the starting material remained. Themixture was cooled to RT and poured into EA/H₂O (2 L/800 mL). Theorganic layer was collected and washed with water (400 mL×2), brine (500mL×2), dried over Na₂SO₄, filtered and concentrated in vacuo. Theresidue was purified by chromatography (PE:EA=10:0 to 1:1) to give 54d(8.00 g, 34%) as a yellow oil and recovered starting material (7.0 g,20%). LC-MS (Waters): R₁ 5.73 min; m/z calculated for C₁₆H₁₈N₂O₄ [M+H]⁺303.1, [M+Na]⁺ 325.1, found [M+H]⁺ 303.1, [M+Na]⁺ 325.1.

5. Procedure for the Preparation of 54e

Acetyl chloride (20.8 g, 0.264 mol) was added to MeOH (40 mL) drop-wiseat 0° C. and the mixture was stirred at RT for 1 h. 54d (8.00 g, 26.4mmol) was then added and stirring was continued at RT for 2 days, TLC(PE:EA=4:1) showed that the starting material was consumed. The reactionwas neutralised with solid NaHCO₃ until pH 7 and the mixture wasfiltered. The filtrate was concentrated in vacuo and the residue waspartitioned between water (30 mL) and EA (30 mL). The organic layer wascollected, washed with brine (30 mL×2), dried over Na₂SO₄, filtered andconcentrated in vacuo. The residue was purified by chromatography(PE:EA=10:1 to 3:1) to give 54e (7.5 g, 88%) as a brown oil. LC-MS(Waters): R_(t) 5.81 min; m/z calculated for C₁₆H₁₉NO₆ [M+H]⁺ 322.1,[M+Na]⁺ 344.1, found [M+H]⁺ 322.2, [M+Na]⁺ 344.1.

6. Procedure for the Preparation of 54f

The following procedure was carried out in five parallel reactions using54e (total of 7.5 g, 23.3 mmol): To a solution of 54e (1.5 g, 4.67 mmol)in THF (10 mL) at 0° C. was added a 1 M aqueous NaOH solution (4.7 mL,4.7 mmol) and the mixture was stirred at 0° C. for 30 min, then allowedto warm to RT and stirred for a further 1 h, LCMS showed most of thestarting material was consumed. The five reaction mixtures were combinedand concentrated in vacuo to remove most of the THF and the residue wasdissolved in a saturated aqueous NaHCO₃ solution and washed with ether.The aqueous layer was acidified to pH 3-4 with a 3 M aqueous HClsolution and extracted with EA. The organic layer was dried over Na₂SO₄,filtered and concentrated in vacuo to give 54f (6.3 g, 86%) as a yellowoil. LC-MS (Agilent, P-2): R_(t) 3.71 min; m/z calculated for C₁₅H₁₇NO₆[M+Na]⁺ 330.1, found [M+Na]⁺ 330.1.

7. Procedure for the Preparation of 54 g

To a stirred solution 54f (3.80 g, 12.4 mmol) in THF (30 mL) at 0° C.under a N₂ atmosphere was added BH₃.THF (1 M solution in THF, 37 mL, 37mmol) and the mixture was stirred at 0° C. for 30 min, TLC(DCM:MeOH=10:1) showed that the starting material was consumed. Thereaction was quenched with MeOH followed by a 3 M aqueous HCl solutionand the mixture was concentrated in vacuo to remove most of THF. Theresidue was partitioned between EA and brine, the organic layer wasseparated, dried over Na₂SO₄, filtered and concentrated in vacuo to give54 g (3.2 g, 88%) as a colorless oil. LC-MS (Agilent, P-2): R_(t) 2.82min; m/z calculated for C₁₅H₁₉NO₅ [M+H]⁺ 294.1, found [MA-1]⁺ 294.1.

8. Procedure for the Preparation of 541,

A mixture of 54 g (3.20 g, 11 mmol) and 10% Pd(OH)₂/C (300 mg) in MeOH(30 mL) was stirred at RT under a H₂ atmosphere (1 atm) overnight, TLC(DCM:MeOH=10:1) showed that the starting material was consumed. Themixture was filtered, the filtrate was concentrated in vacuo and theresidue was dissolved in EA/H₂O (20 mL/20 mL) then cooled to 0° C. KHCO₃(2.75 g, 2.75 mmol) was added followed by diphenyl acetyl chloride (3.0g, 13.2 mmol) and the mixture was stirred at 0° C. for 30 min, TLC(DCM:MeOH=10:1) showed that the starting material was consumed. Theorganic layer was separated, dried over Na₂SO₄, filtered andconcentrated in vacuo. The residue was purified by chromatography(PE:EA=1:0 to 1:1) to give 54 h (2.1 g, 5.5% overall) as a white solid.LC-MS (Agilent, P-2): R_(t) 2.88 min; m/z calculated for C₂₁H₂₃NO₄[M+H]⁺ 354.2, [M+Na]⁺ 376.2, found [M+H]⁺ 354.1, [M+Na]⁺ 376.2.

9. Procedure for the Preparation of 54i

To a solution of 54 h (100 mg, 0.28 mmol) and benzyltrichloroacetimidate (143 mg, 0.56 mmol) in DCM (15 mL) at −10° C. undera N₂ atmosphere was added TMS triflate (18 mg, 0.08 mmol) and themixture was allowed to warm slowly to RT and stirred overnight, TLC(PE:EA=1:1) showed that the starting material was consumed. The mixturewas washed with a saturated aqueous NaHCO₃ solution, brine, dried overNa₂SO₄, filtered and concentrated in vacuo. The residue was purified bychromatography (PE:EA=1:0 to 2:1) to give 54i (90 mg, 72%) as acolorless oil. LC-MS (Agilent, P-2): R_(t) 2.98 min; m/z calculated forC₂₈H₂₉NO₄ [M+H]⁺ 444.2, [M+Na]⁺ 466.2, found [M+H]⁺ 444.2, [M+Na]⁺466.2.

10. Procedure for the Preparation of 54

A mixture of 54i (90 mg, 0.20 mmol) and LiOH.H₂O (25 mg, 0.60 mmol) inTHF/water (3 mL/1 mL) was stirred at RT overnight, TLC (PE:EA=1:1)showed that the starting material was consumed. The mixture wasconcentrated in vacuo, the residue was dissolved in water (10 mL),acidified to pH 3-4 with a 3 M aqueous HCl solution and extracted withDCM. The organic extracts were washed with brine, dried over Na₂SO₄,filtered and concentrated in vacuo. The residue was purified bypreparative HPLC to give 54 (57 mg, 68%) as a white solid. LC-MS(Agilent, P-2): R_(t) 3.09 min; m/z calculated for C₂₇H₂₇NO₄ [M+H]⁺430.2, found [M+H]⁺ 430.3. HPLC (JULY-L) (214 and 254 nm): R_(t) 9.14min. HPLC (ZSJ-2) (214 and 254 nm): R_(t) 20.56 min.

Example 60: Compound 56(2S,4S)-1-(2,2-diphenylacetyl)-4-5-phenyloxazol-2-yl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 56b

To a stirred solution of 56a (0.5 g, 1.63 mmol) in DMF (20 mL) was addedDIPEA (0.63 mL, 4.89 mmol) and HATU (0.74 g, 1.96 mmol) and the mixturewas stirred at RT for 30 min. 2-amino-1-phenylethanone hydrochloride(0.36 g, 2.12 mmol) was then added and stirring was continued at RTovernight, TLC (PE:EA=1:1) showed that the starting material wasconsumed. The mixture was poured into ice-water (40 mL), extracted withEA (40 mL×2) and the combined organic extracts were washed with brine,dried over Na₂SO₄, filtered and concentrated in vacuo. The residue waspurified by chromatography (PE:EA=1:0 to 1:1) to give 56b (260 mg, 37%)as a thick oil. LC-MS (Waters): R_(t) 5.99 min; ink calculated forC₂₃H₂₄N₂O₆ [M+H]⁺ 425.2, [M+Na]⁺ 447.2, found [M+H]⁺ 425.2, [M+Na]⁺447.2.

2. Procedure for the Preparation of 56c

To a solution of 56b (250 mg, 0.59 mmol) in DCM (15 mL) at 0° C. wasadded pyridine (71 mg, 0.89 mmol) then TFAA (0.2 g, 0.71 mmol) and themixture was stirred at 0° C. for 15 min then at RT for 3 hours, TLC(PE:EA=2:1) showed that the starting material was consumed. The reactionwas quenched with a saturated aqueous NaHCO₃ solution, the layers wereseparated and the aqueous layer was extracted with DCM (30 mL×2). Thecombined organic extracts were washed with brine, dried over Na₂SO₄,filtered and concentrated in vacuo. The residue was purified bychromatography (PE:EA=100:0 to 3:1) to give 56c (100 mg, 41%) as a brownoil. LC-MS (Waters): R_(t) 6.93 min; m/z calculated for C₂₃H₂₂N₂O₅[M+H]⁺ 407.2, [M+Na]⁺ 429.2, found [M+H]⁺ 407.2, [M+Na]⁺ 429.2.

3. Procedure for the Preparation of 56d

A mixture of 56c (120 mg, 0.3 mmol) and 10% Pd(OH)₂/C (20 mg) inmethanol (20 mL) was stirred at RT under a H₂ atmosphere (1 atm) for 2h, LC-MS analysis showed that the starting material was consumed. Themixture was filtered and the filtrate was concentrated in vacuo to give56d (60 mg, 75%) as a white solid. LC-MS (Waters): R_(t) 4.97 min; m/zcalculated for C₁₅H₁₆N₂O₃[M+H]⁺ 273.1, found [M+H]⁺ 273.2.

4. Procedure for the Preparation of 56e

To a solution of 56d (60 mg, 0.22 mmol) in DCM (20 mL) at 0° C. wasadded DIPEA (85 mg, 0.66 mmol) then 2,2-diphenylacetyl chloride (76 mg,0.33 mmol) and the mixture was allowed to warm to RT and stirred for 30min, TLC (PE:EA=2:1) showed that the starting material was consumed.Water was added and the mixture was extracted with DCM (30 mL×2). Thecombined organic extracts were washed with brine (20 mL×2), dried overNa₂SO₄, filtered and concentrated in vacuo. The residue was purified bychromatography (PE:EA=10:1 to 3:1) to give 56e (56 mg, 55%) as a yellowoil. LC-MS (Waters): R_(t) 7.02 min; m/z calculated for C₂₉H₂₆N₂O₄[M+H]⁺467.2, found [M+H]⁺ 467.2.

5. Procedure for the Preparation of 56

A mixture of 56e (56 mg, 0.12 mmol) and LiOH.H₂O (16 mg, 0.38 mmol) inTHF/H₂O (2.5 mL/0.5 mL) was stirred at RT overnight. The mixture wasconcentrated in vacuo, the residue was dissolved in water, acidified topH 4˜5 with a 3 M aqueous HCl solution and extracted with DCM (30 mL×3).The combined organic extracts were washed with brine, dried over Na₂SO₄,filtered and concentrated in vacuo. The residue was purified bypreparative HPLC to give 56 (30 mg, 55%) as a white solid. LC-MS(Agilent, P-2): R_(t) 3.00 min; m/z calculated for C₂₈H₂₄N₂O₄ [M+H]⁺453.2, found [M+H]⁺ 453.2. HPLC (JULY-L) (214 and 254 nm): R_(t) 9.12min. HPLC (ZSJ-2) (214 and 254 nm): R_(t) 20.50 min.

Example 61: Compound 120(2S,4S)-1-(2,2-diphenylacetyl)-4-((phenethylthio)methyl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 120b

A mixture of 120a (600 mg, 1.39 mmol), 2-phenylethanethiol (385 mg, 2.78mmol) and Cs₂CO₃ (906 mg, 2.78 mmol) in DMF (10 mL) was heated at 80° C.overnight, TLC (PE:EA=1:1) showed the starting material was consumed.The mixture was poured into ice-water (50 mL) and extracted with EA (20mL×2). The combined organic extracts were washed with brine (25 mL×2),dried over Na₂SO₄, filtered and concentrated in vacuo. The residue waspurified by chromatography (PE:EA=10:1 to 3:1) to give 120b (197 mg,30%) as a colorless oil. LC-MS (Agilent, P-2): R_(t) 3.30 min; m/zcalculated for C₂₉H₃₁NO₃S [M+H]⁺ 474.2, found [M+H]⁺ 474.2.

2. Procedure for the Preparation of 120

Hydrolysis of 120b (70 mg, 0.15 mmol) was performed as described inExample 60, 5. with about 3 equivalents of LiOH.H₂O (18 mg, 0.44 mmol)to give 120 (60 mg, 88%) as a white solid. LC-MS (Agilent, P-2): R_(t)3.21 min; m/z calculated for C₂₈H₂₉NO₃S [M+H]⁺ 460.2, found [M+H]⁺460.2. HPLC (JULY-L) (214 and 254 nm): R_(t) 9.35 min. HPLC (ZSJ-2) (214and 254 nm): R_(t) 22.86 min.

Example 62: Compound 58(2S,S)-1-(2,2-diphenylacetyl)-4-((phenethylsulfonyl)methyl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 58a

To a solution of 120b (120 mg, 0.25 mmol) in DCM (6 mL) was added 80%m-CPBA (137 mg, 0.63 mmol) and the mixture was stirred at RT overnight,TLC (PE:EA=2:1) showed that the starting material was consumed. Themixture was washed with a saturated aqueous Na₂CO₃ solution, brine (10mL), dried over Na₂SO₄, filtered and concentrated in vacuo. The residuewas purified by chromatography (PE:EA=8:1 to 1.5:1) to give 58a (102 mg,82%) as a white solid. LC-MS (Agilent, P-2): R_(t) 2.98 min; m/zcalculated for C₂₉H₃₁NO₅S [M+H]⁺ 506.2, [M+Na]⁺ 528.2, found [M+H]⁺506.2, [M+Na]⁺ 528.2.

2. Procedure for the Preparation of 58

A mixture of 58a (102 mg, 0.20 mmol) and LiOH.H₂O (25 mg, 0.60 mmol) inTHF/H₂O (4 mL/1 mL) was stirred at RT overnight, TLC (PE:EA=1:1) showedthat the starting material was consumed. The mixture was concentrated invacuo, the residue was dissolved in water (4 mL), acidified to pH 4˜5with a 3 M aqueous HCl solution and the resulting precipitate wascollected by filtration and dried at 60° C. to give 58 (77 mg, 77%) as awhite solid. LC-MS (Agilent, P-2): R_(t) 2.77 min; m/z calculated forC₂₈H₂₉NO₅S [M+H]⁺ 492.2, [M+Na]⁺ 514.2, found [M+H]⁺ 492.2, [M+Na]⁺514.2. HPLC (JULY-L) (214 and 254 nm): R_(t) 8.89 min. HPLC (ZSJ-2) (214and 254 nm): R_(t) 18.32 min.

Example 63: Compound 121(2S,4S)-4-((benzylthio)methyl)-1-(2,2-diphenylacetyl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 121a

A mixture of 120a (600 mg, 1.39 mmol), BnSH (345 mg, 2.78 mmol) andCs₂CO₃ (906 mg, 2.78 mmol) in DMF (10 mL) was heated at 80° C.overnight, TLC (PE:EA=1:1) showed that the 120a was consumed. Themixture was poured into ice-water (50 mL) and extracted with EA (20mL×2). The combined organic extracts were washed with brine (15 mL×2),dried over Na₂SO₄, filtered and concentrated in vacuo. The residue waspurified by chromatography (PE:EA=10:1 to 4:1) to give 121a (140 mg,21%) as colorless oil. LC-MS (Agilent, P-2): R_(t) 3.10 min; m/zcalculated for C₂₈H₂₉NO₃S [M+H]⁺ 460.2, found [M+H]⁺ 460.2.

2. Procedure for the Preparation of 121

A mixture of 121a (56 mg, 0.12 mmol) and LiOH.H₂O (15 mg, 0.37 mmol) inTHF/H₂O (3 mL/1 mL) was stirred at RT overnight, TLC (PE:EA=2:1) showedthat the starting material was consumed. The mixture was concentrated invacuo, the residue was dissolved in water (10 mL), acidified to pH 4˜5with a 3 M aqueous HCl solution and extracted with DCM (10 mL×2). Thecombined organic extracts were washed with brine (10 mL), dried overNa₂SO₄, filtered and concentrated in vacuo to give 121 (50 mg, 92%) aswhite solid. LC-MS (Agilent, P-2): R_(t) 3.16 min; m/z calculated forC₂₇H₂₇NO₃S [M+H]⁺ 446.2, found [M+H]⁺ 446.2. HPLC (JULY-L) (214 and 254nm): R_(t) 9.26 min. HPLC (ZSJ-2) (214 and 254 nm): R_(t) 21.92 min.

Example 64: Compound 122(2S,4S)-1-(2,2-diphenylacetyl)-4-((phenylthio)methyl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 120a

To a solution of 54 h (1.90 g, 5.37 mmol) and Et₃N (0.71 g, 6.98 mmol)in DCM (15 mL) at 0° C. was added MsCl (0.67 g, 5.91 mmol) and themixture was stirred at 0° C. for 30 min, TLC (PE:EA=1:1) showed that thestarting material was consumed. The mixture was washed with brine, driedover Na₂SO₄, filtered and concentrated in vacuo. The residue waspurified by chromatography (PE:EA=1:0 to 1:1) to give 120a (2.2 g, 95%)as a white solid. LC-MS (Agilent, P-2): R_(t) 2.85 min; m/z calculatedfor C₂₂H₂₆NO₆S [M+H]⁺ 432.2, [M+Na]⁺ 454.1, found [M+H]⁺ 432.2, [M+Na]⁺454.1.

2. Procedure for the Preparation of 122a

A mixture of 120a (500 mg, 1.39 mmol), and PhSNa (229 mg, 1.74 mmol) inDMF (10 mL) was heated at 80° C. overnight, TLC (PE:EA=2:1) showed thatmost of the starting material was consumed. The mixture was cooled toRT, poured into ice-water (60 mL) and extracted with EA (20 mL×3). Thecombined organic extracts were washed with brine, dried over Na₂SO₄,filtered and concentrated in vacuo. The residue was purified bychromatography (PE:EA=1:0 to 2:1) to give 122a (150 mg, 29%) as aviscous colorless oil. LC-MS (Agilent, P-2): R_(t) 3.30 min; m/zcalculated for C₂₇H₂₇NO₃S [M+H]⁺ 446.2, found [M+H]⁺ 446.2.

3. Procedure for the Preparation of 122

A mixture of 122a (50 mg, 0.11 mmol) and LiOH.H₂O (14 nag, 0.33 mmol) inTHF/H₂O (3 mL/1 mL) was stirred at RT overnight, TLC (PE:EA=2:1) showedthat the starting material was consumed. The mixture was concentrated invacuo and the residue was dissolved in water (10 mL), washed with etherthen acidified to pH 3˜4 with a 3 M aqueous HCl solution and extractedwith DCM. The organic extracts were washed with brine, dried overNa₂SO₄, filtered and concentrated in vacuo to give 122 (30 mg, 62%) as awhite solid. LC-MS (Agilent, P-2): R_(t) 3.18 min; m/z calculated forC₂₆H₂₅NO₃S [M+H]⁺ 432.2, [M+Na]+454.2, found [M+H]⁺ 432.2, [M+Na]⁺454.1. HPLC (JULY-L) (214 and 254 nm): R_(t) 9.24 min. HPLC (ZSJ-2) (214and 254 nm): R_(t) 21.70 min.

Example 65: Compound 126(2S,4S)-1-(2,2-diphenylacetyl)-4-((2-fluorophenoxy)ethyl)(methyl)amino)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 126a

A mixture of 90c (50 mg, 0.14 mmol), Cs₂CO₃ (68 mg, 0.21 mmol) and4-fluorophenylethylbromide (37 mg, 0.17 mmol) in DMF (2 mL) was heatedat 70° C. overnight, TLC (DCM:MeOH=20:1) showed that the startingmaterial was consumed. The mixture was cooled to RT, partitioned betweenEA (30 mL) and H₂O (30 mL) and the organic layer was separated, washedwith brine, dried over Na₂SO₄, filtered and concentrated in vacuo. Theresidue was purified by chromatography (PE:EA=10:1 to 1:2) to give 126a(40 mg, 58%) as a yellow oil. LC-MS (Waters): R_(t) 6.07 min; m/zcalculated for C₂₉H₃₁FN₂O₄ [M+H]⁺ 491.1, found [M+H]⁺ 491.1.

2. Procedure for the Preparation of 126

A mixture of 126a (127 mg, 0.26 mmol) and LiOH.H₂O (44 mg, 1.04 mmol) inTHF/H₂O (3 mL/0.5 mL) was stirred at RT overnight, TLC (DCM:MeOH=20:1)showed that the starting material was consumed. The mixture wasconcentrated in vacuo, the residue was dissolved in H₂O (3 mL),acidified to pH 5 with a 3 M aqueous HCl solution and extracted with DCM(10 mL×2). The combined organic extracts were dried over Na₂SO₄,filtered and concentrated in vacuo. The residue was purified bypreparative HPLC to give 126 (20 mg, 18%) as a white solid. LC-MS(Agilent, P-2): R_(t) 2.824 min; m/z calculated for C₂₈H₂₉FN₂O₄ [M+H]⁺477.2, found [M+H]⁺ 477.2. HPLC (ZSJ-2) (214 and 254 nm)): R_(t) 16.13min.

Example 66: Compound 133(2S,4S)-1-(2,2-diphenylacetyl)-4((3-(4-fluorophenyl)propyl)thio)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 133a

To a solution of 3-(4-fluorophenyl) propanoic acid (6.0 g) in THF (30mL) at 0° C. under a N₂ atmosphere was added BH₃.THF (1 M in THF, 42.8mL, 42.8 mmol) dropwise and the mixture was allowed to warm slowly to RTand stirred for 3 h, TLC (PE:EA=2:1) showed that the starting materialwas consumed. The mixture was re-cooled to 0° C., quenched with MeOH (5mL) then water (10 mL) and concentrated in vacuo. The residue wasdiluted with water (20 mL) and extracted with EA. The organic phase waswashed with a saturated aqueous NaHCO₃ solution (20 mL) then brine,dried over Na₂SO₄, filtered and concentrated in vacuo to give 133a (5.0g, 90%) as a colorless oil.

2. Procedure for the Preparation of 1336

To a solution of 133a (937 mg, 6.08 mmol) and PPh₃ (1.59 g, 6.08 mmol)in THF (20 mL) at 0° C. was added CBr₄ (2.11 g, 6.38 mmol) in portionsand the mixture was allowed to warm slowly to RT and stirred for 3 h,TLC (PE:EA=10:1) showed that most of the starting material was consumed.The mixture was filtered the filtrate was concentrated in vacuo. Theresidue was purified by chromatography (100% PE) to give 133b (724 mg,54%) as a colorless oil.

3. Procedure for the Preparation of 133c

To a solution of 124b (202 mg, 0.57 mmol) in DMF (10 mL) was added K₂CO₃(87 mg, 0.63 mmol) and 133b (136 mg, 0.63 mmol) and the mixture washeated at 80° C. overnight, TLC (PE:EA=2:1) showed that the startingmaterial was consumed. The mixture was poured into ice-water (30 mL) andextracted with EA (15 mL×2). The combined organic extracts were washedwith brine (30 mL), dried over Na₂SO₄, filtered and concentrated invacuo. The residue was purified by chromatography (PE:EA=8:1 to 5:1) togive 133c (232 mg, 83%) as a colorless oil. LC-MS (Agilent, P-2): R_(t)3.26 min; m/z calculated for C₂₉H₃₀FNO₃S [M+H]⁺ 492.2, found [M+H]⁺492.2.

4. Procedure for the Preparation of 133

A mixture of 133c (105 mg, 0.21 mmol) and LiOH.H₂O (27 mg, 0.63 mmol) inTHF/H₂O (3 mL/1 mL) was stirred at RT overnight, TLC (PE:EA=1:1) showedthat the starting material was consumed. The mixture was concentrated invacuo, the residue was dissolved in water (10 mL), acidified to pH 4˜5with a 3 M aqueous HCl solution and extracted with DCM. The organiclayer was washed with brine, dried over Na₂SO₄, filtered andconcentrated in vacuo to give 133 (100 mg, 98%) as a white solid. LC-MS(Agilent, P-2): R_(t) 3.29 min; m/z calculated for C₂₈H₂₈FNO₃S [M+H]⁺478.2, found [M+H]⁺ 478.2. HPLC (JULY-L) (214 and 254 nm): R_(t) 9.34min.

Example 67: Compound 134(2S,4S)-1-(2,2-diphenylacetyl)-4((3-(4-fluorophenyl)propyl)sulfonyl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 134a

To a solution of 133c (105 mg, 0.21 mmol) in DCM (5 mL) was added 80%m-CPBA (115 mg, 0.53 mmol) and the mixture was stirred at RT overnight,TLC (PE:EA=1:1) showed that the starting material was consumed. Thereaction was quenched with a saturated aqueous NaHSO₃ solution and themixture was washed with a saturated aqueous Na₂CO₃ solution (5 mL), thenbrine (5 mL), dried over Na₂SO₄, filtered and concentrated in vacuo. Theresidue was purified by chromatography (PE:EA=8:1 to 2:1) to give 134a(100 mg, 90%) as a colorless oil. LC-MS (Agilent, P-2): R_(t) 3.04 min;m/z calculated for C₂₉H₃₀FNO₅S [M+H]⁺ 524.2, [M+Na]⁺ 546.2, found [M+H]⁺524.2, [M+Na]⁺ 546.2.

2. Procedure for the Preparation of 134

A mixture of 134a (100 mg, 0.19 mmol) and LiOH.H₂O (24 mg, 0.57 mmol) inTHF/H₂O (3 mL/1 mL) was stirred at RT overnight, TLC (PE:EA=1:1) showedthat the starting material was consumed. The mixture was concentrated invacuo, the residue was dissolved in water (3 mL), washed with Et₂O thenacidified to pH 4˜5 with a 3 M aqueous HCl solution. The resultingprecipitate was collected by filtration and dried at 55° C. to give 134(60 mg, 61%) as a white solid. LC-MS (Agilent, P-2): R_(t) 2.94 min; m/zcalculated for C₂₈H₂₈FNO₅S [M+H]⁺ 510.2, [M+Na]⁺ 532.2, found [M+H]⁺510.2, [M+Na]⁺ 532.2. HPLC (JULY-L) (214 and 254 nm): R_(t) 8.91 min.

Example 68: Compound 136(2S,4S)-1-(2,2-diphenylacetyl)-4-((3-(4-fluorophenyl)propyl)(methyl)amino)pyrrolidine-2-carboxamide

To a solution of 91 (1.2 g, 2.53 mmol) in DMF (20 mL) was added DIPEA(645 mg, 5.03 mmol) and HATU (1.54 g, 4.05 mmol) and the mixture wasstirred at RT for 1 h. A 37% aqueous NH₄OH solution (1 mL) was thenadded and stirring was continued at RT overnight, TLC (DCM:MeOH=10:1)showed that the starting material was consumed. Water (30 mL) was addedand the mixture was extracted with EA (30 mL×3). The combined organiclayers were washed with brine, dried over Na₂SO₄, filtered andconcentrated in vacuo. The residue was purified by column chromatography(DCM:MeOH=1:0 to 20:1) to afford 136 (500 mg, 40%) as a white solid.LC-MS (Agilent, P-2): R_(t) 2.825 min; m/z calculated for C₂₉H₃₂FN₃O₂[M+H]⁺ 474.3, found [M+H]⁺ 474.3. HPLC (JULY-L) (214 and 254 nm): R_(t)9.032 min.

Example 69: Compound 137(2S,4S)-1-(2,2diphenylacetyl)-4-((3-(4-fluorophenyl)propyl)(methyl)amino)pyrrolidine-2-carbonitrile

To a solution of 136 (430 mg, 0.91 mmol) in DCM (5 mL) at 0° C. wasadded TEA (139 mg, 1.37 mmol) and the mixture was stirred at 0° C. for15 min. TFAA (231 mg, 1.1 mmol) was then added drop-wise at 0° C. andthe mixture was stirred at that temperature for 30 min before allowingto warm slowly to RT and stirred overnight, TLC (PE:EA=1:2) showed thatthe starting material was consumed. The reaction was quenched with asaturated aqueous NaHCO₃ solution, the layers were separated and theaqueous layer was extracted with DCM (15 mL×2). The combined organiclayers were washed with brine (15 mL), dried over Na₂SO₄, filtered andconcentrated in vacuo. The residue was purified by column chromatography(PE:EA=10:1 to 1:1) to give 137 (320 mg, 77%) as a brown oil. LC-MS(Agilent, P-2): R_(t) 2.761 min; m/z calculated for C₂₉H₃₀FN₃O [M+H]⁺456.2, found [M+H]⁺ 456.2. HPLC (JULY-L) (214 and 254 nm): R_(t) 8.894min.

Example 70: Compound 1381-(2S,4S)-4-((3-(4-fluorophenyl)propyl)(methyl)amino)-2-(1H-tetrazol-5-yl)pyrrolidin-1-yl)-2,2-diphenylethanoate

To a solution of 137 (240 mg, 0.53 mmol) in DMF (3 mL) was added NaN₃(172 mg, 2.64 mmol) and NH₄Cl (192 mg, 3.55 mmol) and the flask wassealed and heated at 100° C. overnight, TLC (DCM:MeOH=50:1) showed thatthe starting material was consumed. The mixture was partitioned betweenEA (30 mL) and water (30 mL), the organic layer was collected and washedwith brine, dried over Na₂SO₄, filtered and concentrated in vacuo. Theresidue was purified by chromatography (DCM:MeOH=20:1) to afford 138(165 mg, 65%) as a white solid. LC-MS (Agilent, P-2): R_(t) 2.879 min;m/z calculated for C₂₉H₃₁FN₆O [M+H]⁺ 499.3, found [M+H]⁺ 499.3. HPLC(JULY-L) (214 and 254 nm): R_(t) 8.871 min.

Example 71: Compound 135(2S,4S)-1-(2,2-diphenylacetyl)-N-(methylsulfonyl)-4-(phenylpropoxy)pyrrolidine-2-carboxamide

1. Procedure for the Preparation of Compound 135b

To a stirred solution of 135a (20 mg, 0.057 mmol) in DCM (0.2 mL) wasadded MeSO₂NH₂ (6 mg, 0.062 mmol), DCC (14 mg, 0.068 mmol) and DMAP (2.0mg, 0.017 mmol). The flask was sealed and the mixture was stirred at RTfor 2 days, LCMS analysis showed that the starting material wasconsumed. The mixture was concentrated in vacuo to give 135b (50 mg) asa white solid, which was used directly in the next step withoutpurification. LC-MS (Agilent, P-2): R_(t) 2.78 min; m/z calculated forC₂₀H₃₀N₂O₆S [M+Na]⁺ 449.2, found [M+Na]⁺ 449.3.

2. Procedure for the Preparation of 135

A mixture of 135b (50 mg, assumed 0.057 mmol) and a 4 M HCl/MeOHsolution (5 mL) was stirred at RT overnight, LCMS analysis showed thatthe starting material was consumed. The mixture was concentrated invacuo, the residue was dissolved in water, basified to pH 8 with K₂CO₃and extracted with DCM. The organic layer was then dried over Na₂SO₄ andfiltered. To the filtrate was added Et₃N (9 mg, 0.085 mmol) thendiphenyl acetyl chloride (16 mg, 0.068 mmol) and the mixture was stirredat RT for 1 h, TLC (DCM:MeOH=10:1) showed a that a major new productformed. The mixture was washed with a 20% aqueous K₂CO₃ solution, brine,dried over Na₂SO₄, filtered and concentrated in vacuo. The residue waspurified by preparative HPLC to give 135 (11 mg, 38% over three steps)as a white solid. LC-MS (Agilent, P-2): R_(t) 2.68 min; m/z calculatedfor C₂₉H₃₂N₂O₅S [M+H]⁺ 521.2, found [M+H]⁺ 521.2. HPLC (JULY-L) (214 and254 nm): R_(t) 9.17 min.

Example 72: Compound 131(2S,4S)-1-(2,2-diphenylacetyl)-4-(phenethylthio)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 131a

A mixture of 124b (190 mg, 0.53 mmol), 1-(2-bromoethyl)benzene (109 mg,0.58 mmol) and K₂CO₃ (81 mg, 0.58 mmol) in DMF (10 mL) was heated at 80°C. overnight, TLC (PE:EA=2:1) showed that the starting material wasconsumed. The mixture was cooled to RT, poured into ice-water (60 mL)and extracted with ether (30 mL×2). The combined organic extracts werewashed with brine, dried over Na₂SO₄, filtered and concentrated invacuo. The residue was purified by chromatography (PE:EA=1:0 to 4:1) togive 131a (200 mg, 83%) as a colorless oil. LC-MS (Agilent, P-2): R_(t)3.15 min; m/z calculated for C₂₈H₂₉NO₃S [M+H]⁺ 460.2, found [M+H]⁺460.2.

2. Procedure for the Preparation of 131

A mixture of 131a (80 mg, 0.17 mmol) and LiOH.H₂O (29 mg, 0.69 mmol) inTHF/water (3 mL/1 mL) was stirred at RT overnight, TLC (PE:EA=2:1)showed that the starting material was consumed. The mixture wasconcentrated in vacuo, the residue was dissolved in water (10 mL),acidified to p=3-4 with a 3 M aqueous HCl solution and extracted withDCM (10 mL×2). The combined organic extracts were washed with brine,dried over Na₂SO₄, filtered and concentrated in vacuo to give 131 (70mg, 93%) as a white solid. LC-MS (Agilent, P-2): R_(t) 3.20 min; m/zcalculated for C₂₇H₂₇NO₃S [M+H]⁺ 446.2, found [M+H]⁺ 446.2. HPLC(JULY-L) (214 and 254 nm): R_(t) 9.27 min.

Example 73: Compound 132(2S,4S)-1-(2,2-diphenylacetyl)-4-(phenethylsufonyl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 132a

To a stirred solution of 131a (120 mg, 0.26 mmol) in DCM (10 mL) at 0°C. was added 80% m-CPBA (140 mg, 0.65 mmol) in three portions and themixture was allowed to warm slowly to RT and stirred overnight, TLC(PE:EA=2:1) showed that the starting material was consumed. The mixturewas washed with a saturated aqueous Na₂CO₃ solution (5 mL×2), brine (5mL×2) then dried over Na₂SO₄, filtered and concentrated in vacuo. Theresidue was purified by chromatography (PE:EA=1:9 to 3:1) to give 132a(110 mg, 86%) as a colorless oil. LC-MS (Agilent, P-2): R_(t) 3.01 min;m/z calculated for C₂₈H₂₉NO₅S [M+H]⁺ 492.2, [M+Na]⁺ 514.2, found [M+H]⁺492.2, [M+Na]⁺ 514.2.

2. Procedure for the Preparation of 132

A mixture of 132a (110 mg, 0.22 mmol) and LiOH.H₂O (37 mg, 0.88 mmol) inTHF/water (3 mL/1 mL) was stirred at RT overnight, TLC (PE:EA=1:1)showed that the starting material was consumed. The mixture wasconcentrated in vacuo, the residue was dissolved in water (10 mL) andacidified to pH 3-4 with a 3 M aqueous HCl solution. The resultingprecipitate was collected by filtration then dried to give 132 (80 mg,77%) as a white solid. LC-MS (Agilent, P-2): R₁ 2.84 min; m/z calculatedfor C₂₇H₂₇NO₅S [M+H]⁺ 478.2, found [M+H]⁺ 478.2. HPLC (JULY-L) (214 and254 nm): R₁ 8.84 min.

Example 74: Compound 118(2S,4S)-4-((benzylsulfonyl)methyl)-1-(diphenylacetyl)-pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 118a

To a solution of 121a (80 mg, 0.17 mmol) in DCM (6 mL) was added 80%m-CPBA (94 mg, 0.43 mmol) and the mixture was stirred at RT overnight,TLC (PE:EA=2:1) showed that the 121a was consumed. The mixture waswashed with a saturated aqueous Na₂CO₃ solution, brine (10 mL), driedover Na₂SO₄, filtered and concentrated in vacuo. The residue waspurified by chromatography (PE:EA=8:1 to 1.5:1) to give 118a (77 mg,90%) as a white solid. LC-MS (Agilent, P-2): R_(t) 3.12 min; m/zcalculated for C₃₁H₃₂N₂O₃ [M+H]⁺ 492.2, [M+Na]⁺ 514.2, found [M+H]⁺492.2, [M+Na]⁺ 514.2.

2. Procedure for the Preparation of 118

A mixture of 118a (77 mg, 0.16 mmol) and LiOH.H₂O (20 mg, 0.47 mmol) inTHF/H₂O (4 mL/1 mL) was stirred at RT overnight, TLC (PE:EA=1:1) showedthat the starting material was consumed. The mixture was concentrated invacuo, the residue was dissolved in water (5 mL), acidified to pH 4˜5with a 3 M aqueous HCl solution and the resulting precipitate wascollected by filtration and dried at 60° C. to give 118 (40 mg, 54%) asa white solid. LC-MS (Agilent, P-2): R_(t) 2.88 min; m/z calculated forC₂₇H₂₇NO₅S [M+H]⁺ 478.2, [M+Na]⁺ 500.2, found [M+H]⁺ 478.2, [M+Na]⁺500.2. HPLC (JULY-L) (214 and 254 nm): R_(t) 8.75 min. HPLC (ZSJ-2) (214and 254 nm): R_(t) 16.68 min.

Example 75: Compound 119(2S,4S)-4-((phenylsulfonyl)methyl)-1-(diphenylacetyl)-pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 119a

To a solution of 122b (80 mg, 0.18 mmol) in DCM (5 mL) at 0° C. wasadded 80% m-CPBA (97 mg, 0.45 mmol) and the mixture was allowed to warmslowly to RT and stirred for 3 h, TLC (PE:EA=1:1) showed that thestarting material was consumed. A saturated aqueous Na₂CO₃ solution wasadded, the layers were separated and the aqueous layer was extractedwith DCM (20 mL×3). The combined organic extracts were washed withbrine, dried over Na₂SO₄, filtered and concentrated in vacuo. Theresidue was purified by chromatography (PE:EA=1:0 to 1:1) to give 119a(55 mg, 64%) as a white solid. LC-MS (Waters): R_(t) 6.27 min; m/zcalculated for C₂₇H₂₇NO₅S [M+H]⁺ 478.0, [M+Na]⁺ 500.1 found [M+H]⁺478.0, [M+Na]⁺ 500.0.

2. Procedure for the Preparation of 119

A mixture of 119a (55 mg, 0.12 mmol) and LiOH.H₂O (15 mg, 0.35 mmol) inTHF/H₂O (2 mL/0.5 mL) was stirred at RT overnight, TLC (PE:EA=1:1)showed that the starting material was consumed. The mixture wasconcentrated in vacuo, the residue was dissolved in water, acidified topH 3˜4 with a 3 M aqueous HCl solution and the resulting precipitate wascollected by filtration then purified by preparative HPLC to give 119(30 mg, 50%) as a white solid. LC-MS (Agilent, P-2): R_(t) 2.917 min;m/z calculated for C₂₆H₂₅NO₅S [M+H]⁺ 464.2, found [M+H]⁺ 464.2. HPLC(JULY-L) (214 and 254 nm): R_(t) 8.73 min. HPLC (ZSJ-2) (214 and 254nm): R_(t) 16.36 min.

Example 76: Compound 114(2S,4S)—N—(N,N-dimethylsulfamoyl)-1-(2,2-diphenylacetyl)-4-((3-(4-fluorophenyl)propyl)(methyl)amino)pyrrolidine-2-carboxylicacid

To a solution of 91 (100 mg, 0.21 mmol) in DCM (5 mL) was addedN,N-dimethylsulfamide (28.8 mg, 0.23 mmol), DMAP (6.3 mg, 0.063 mmol)and DCC (52 mg, 0.25 mmol) and the mixture was stirred at RT for 72 h,TLC (DCM:MeOH=20:1) showed that the starting material was consumed. Themixture was filtered, the filtrate was concentrated in vacuo and theresidue was purified by preparative HPLC to give 114 (56 mg, 46%) as awhite solid. LC-MS (Agilent, P-2): R_(t) 2.86 min; m/z calculated forC₃₁H₃₇FN₄O₄S [M+H]⁺ 581.3, found [M+H]⁺ 581.3. HPLC (JULY-L) (214 and254 nm): R_(t) 8.88 min.

Example 77: Compound 146(2S,4S)-1-(2,2-diphenylacetyl)-4-methyl(prop-2-yn-1-yl)amino)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 146a

To a solution of 90c (200 mg, 0.57 mmol) in DMF (8 mL) was added Cs₂CO₃(222 mg, 0.68 mmol) then 3-bromoprop-1-yne (68 mg, 0.57 mmol). The flaskwas sealed and the mixture was heated at 40° C. overnight, TLC(PE:EA=1:2) showed that the starting material was consumed. The mixturewas poured into ice-water (30 mL) and extracted with EA (15 mL×4). Thecombined organic extracts were washed with brine, dried over Na₂SO₄,filtered and concentrated in vacuo. The residue was purified bychromatography (PE:EA=10:1 to 3:1) to give 146a (61 mg, 27%) as acolorless oil. LC-MS (Agilent, P-2): R_(t) 2.592 min; m/z calculated forC₂₄H₂₆N₂O₃ [M+H]⁺ 391.2, found [M+H]⁺ 391.2.

2. Procedure for the Preparation of 146

A mixture of 146a (61 mg, 0.21 mmol) and LiOH.H₂O (20 mg, 0.47 mmol) inTHF/H₂O (3 mL/1 mL) was stirred at RT overnight, TLC (PE:EA=1:2) showedthat the starting material was consumed. The mixture was concentrated invacuo to remove THF, the residue was dissolved in water (5 mL),acidified to pH 4 with a 4 M aqueous HCl solution and extracted with DCM(5 mL×5). The combined organic extracts were washed with brine, driedover Na₂SO₄, filtered and concentrated in vacuo to give crude 146 (57mg) and 27 mg of this crude material was purified by preparative HPLC togive pure 146 (20 mg, 53%) as a viscous colorless oil. LC-MS (Agilent,P-2): R_(t) 2.51 min; m/z calculated for C₂₃H₂₄N₂O₃ [M+H]⁺ 377.2, found[M+H]⁺ 377.2. HPLC (JULY-L) (214 and 254 nm): R_(t) 8.50 min.

Example 78: Compound 147(2S,4S)-1-(2,2-diphenylacetyl)-4-(methyl(propyl)amino)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 147a

A mixture of 146a (29 mg, 0.074 mmol) and Raney-Ni (50 mg) in EA/EtOH(10 mL/10 mL) was stirred under a H₂ atmosphere (1 atm) at 30° C.overnight, LCMS analysis showed that the starting material was consumed.The mixture was filtered and the filtrate was concentrated in vacuo togive 147a (22 mg, 75%) as a colorless oil. LC-MS (Agilent, P-2): R_(t)2.75 min; m/z calculated for C₂₋₄H₃₀N₂O₃[M+H]⁺ 395.2, found [M+H]⁺395.2.

2. Procedure for the Preparation of 147

A mixture of 147a (22 mg, 0.056 mmol) and LiOH.H₂O (7 mg, 0.168 mmol) inTHF/H₂O (3 mL/1 mL) was stirred at RT for 2 days, LCMS analysis showedthat the starting material was consumed. The mixture was concentrated invacuo to remove the THF, the residue was dissolved in water (5 mL),acidified to pH 4 with a 4 M aqueous HCl solution and concentrated invacuo. The residue was purified by preparative HPLC to give 147 (7 mg,33%) as a white solid. LC-MS (Agilent, P-2): R_(t) 2.47 min; m/zcalculated for C₂₃H₂₈N₂O₃ [M+H]⁺ 381.2, found [M+H]⁺ 381.2. HPLC(JULY-L) (214 and 254 nm): R_(t) 8.55 min.

Example 79: Compound 148((2S,4S)-4-((4,4-dimethylpent-2-yn-1-yl)(methyl)amino)-1-(2,2-diphenylaetyl)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 148a

To a solution of 90c (300 mg, 0.85 mmol) in DMF (8 mL) was added Cs₂CO₃(333 mg, 1.02 mmol) then 4,4-dimethylpent-2-ynyl methanesulfonate (194mg, 1.02 mmol) and the mixture was heated at 40° C. overnight, TLC(PE:EA=1:1) showed that the starting material was consumed. The mixturewas poured into ice-water (30 mL) and extracted with EA (15 mL×3). Thecombined organic extracts were washed with brine (20 mL×2), dried overNa₂SO₄, filtered and concentrated in vacuo. The residue was purified bychromatography (PE:EA=10:1 to 4:1) to give 148a (100 mg, 26%) as acolorless oil. LC-MS (Agilent, P-2): R_(t) 3.60 min; m/z calculated forC₂₈H₃₄N₂O₃ [M+H]⁺ 447.3, found [M+H]⁺ 447.3.

2. Procedure for the Preparation of 148

A mixture of 148a (100 mg, 0.22 mmol) and LiOH.H₂O (28 mg, 0.67 mmol) inTHF/H₂O (5 mL/1 mL) was stirred at RT overnight, TLC (PE:EA=1:1) showedthat the starting material was consumed. The mixture was concentrated invacuo to remove THF, the residue was dissolved in water (5 mL),acidified to pH 4 with a 4 M aqueous HCl solution and extracted with DCM(5 mL×4). The combined organic extracts were washed with brine (10mL×2), dried over Na₂SO₄, filtered and concentrated in vacuo to givecrude 148 (95 mg) and 35 mg of the crude material was purified bypreparative HPLC to give pure 148 (25 mg, 71%) as a white solid. LC-MS(Agilent, P-2): R_(t) 3.08 min; m/z calculated for C₂₇H₃₂N₂O₃ [M+H]⁺433.2, found [M+H]⁺ 433.2. HPLC (JULY-L) (214 and 254 nm): R₁ 9.08 min.

Example 80: Compound 149((2S,4S)-4-((4,4-dimethylpentyl)methyl)amino)-1-(2,2-diphenylacetyl)pyrrolidine-2-carboxylicacid

A mixture of 148 (30 mg, 0.069 mmol) and Raney-Ni (50 mg) in EA/EtOH (10mL/10 mL) was stirred under a H₂ atmosphere (1 atm) at 38° C. overnight,LCMS analysis showed that the starting material was consumed. Themixture was filtered and the filtrate was concentrated in vacuo. Theresidue was purified by preparative HPLC to give 149 (12 mg, 40%) as awhite solid. LC-MS (Agilent, P-2): R_(t) 2.63 min; m/z calculated forC₂₇H₃₆N₂O₃ [M+H]⁺ 4373, found [M+H]⁺ 437.3. HPLC (JULY-L) (214 and 254nm): R_(t) 9.15 min.

Example 81: Compound 16(2S,4S)-1-(2,2-diphenylacetyl)-4-(((1R,2R)-2-phenylcyclopropyl)methoxy)pyrrolidine-2-carboxylicacid and(2S,4S)-1-(2,2-diphenylacetyl)-4-(((1S,2S)-2-phenylcyclopropyl)methoxy)pyrrolidine-2-carboxylicacid

1. Procedure for the Preparation of 16b

A solution of 16a (12.0 g, 48.8 mmol) in 4 M HCl/diox (60 mL) wasstirred at RT overnight, TLC (MeOH:DCM=1:10) showed the startingmaterial was consumed. The mixture was concentrated in vacuo, theresidue was dissolved in water (50 mL) and extracted with diethyl ether(100 mL×2). The aqueous layer was basified to pH=9˜10 with a saturatedaqueous Na₂CO₃ solution and extracted with EA (100 mL×2). The combinedorganic extracts were washed with brine (100 mL×2), dried over Na₂SO₄,filtered and concentrated in vacuo to give 16b as a colorless oil (5.0g, 78%). LC-MS (Agilent): R_(t) 2.81 min; m/z calculated for C₁₉H₁₅NO₃[M+H]⁺ 262.1, [M+Na]⁺ 284.1, found [M+H]⁺ 262.1, [M+Na]⁺ 284.1.

2. Procedure for the Preparation of 16c

To a solution of 16b (300 mg, 1.15 mmol) and Et₃N (175 mg, 1.72 mmol) inDCM (5 mL) was added diphenylacetyl chloride (318 mg, 1.38 mmol) at 0°C. under N₂ and the mixture was stirred at 0° C. for 30 min, TLC(PE:EA=1:1) showed the starting material was consumed. The mixture waswashed with brine (3 mL×2), dried over Na₂SO₄, filtered and concentratedin vacuo. The residue was purified by chromatography (PE:EA=10:0 to 4:1)to give 16c as a thick oil (300 mg, 57%). LC-MS (Agilent): R_(t) 3.38min; m/z calculated for C₂₉H₂₉NO₄ [M+H]⁺ 456.2, [M+Na]⁺ 478.2, found[M+H]⁺ 456.2, [M+Na]⁺ 478.2.

3. Procedure for the Preparation of 16d

A stirred solution of 16c (150 mg, 0.33 mmol) in dry DCE (5 mL) wascooled to 0° C. under a N₂ atmosphere. A ZnEt₂ solution (1 M in hexane,0.66 mL, 0.66 mmol) was added followed by CH₂I₂ (354 mg, 1.32 mmol) andthe mixture was warmed to RT slowly and stirred overnight. The mixturewas re-cooled to 0° C., quenched with a saturated aqueous NH₄Cl solution(10 mL) and extracted with DCM (20 mL). The organic layer was separated,washed with brine, dried over Na₂SO₄ then filtered and concentrated invacuo. The residue was purified by chromatography (PE:EA=4:1) to give16d as a thick oil (120 mg, 78%). LC-MS (Agilent): R_(t) 3.38 min; m/zcalculated for C₃₀H₃₁NO₄ [M+H]⁺ 470.2, [M+Na]⁺ 492.2, found [M+H]⁺470.2, [M+Na]⁺ 492.2.

4. Procedure for the Preparation of 16

To a stirred solution of 16d (110 mg, 0.23 mmol) in THF (3 mL) was addeda solution of LiOH.H₂O (33 mg, 0.79 mmol) in water (1 mL) and themixture was stirred at RT overnight, TLC (PE:EtOAc=1:1) showed thestarting material was consumed. The mixture was concentrated in vacuo toremove most of the THF and the residue was partitioned between DCM (15mL) and water (15 mL). The aqueous layer was acidified with a 1 Maqueous HCl solution to pH=3˜4, the DCM layer was separated and theaqueous layer was extracted again with DCM (15 mL). The combined organicextracts were washed with brine (30 mL×2), dried over Na₂SO₄, filteredand concentrated in vacuo. The residue was purified by flashchromatography (DCM: MeOH=50:1 to 20:1) to give the product as a whitesolid (80 mg, 77%). LC-MS (Agilent): R_(t) 3.39 min; m/z calculated forC₂₉H₂₉NO₄ [M+H]⁺ 456.2, [M+Na]⁺ 478.2, found [M+H]⁺ 456.2, [M+Na]⁺478.2. HPLC (214 and 254 nm): 13.75 min.

Example 82: Compound 84(2S,4S)-4-((4aS,7aS)-6-benzoctahydro-1H-pyrrolo[3,4-b]pyridin-1-yl)-1-(2,2-diphenylacetyl)pyrrolidine-2-carboxylicacid

6. Procedure for the Preparation of 84a

A solution of the amine (257 mg, 0.89 mmol) in DCE (10 mL) was cooled to0° C. and Et₃N (181 mg, 1.78 mmol) was added followed by a solution of28a (300 mg, 0.89 mmol) in DCE (5 mL). AcOH (0.5 mL) and the mixture wasstirred at RT for 30 min. NaBH(OAc)₃ (282 mg, 1.34 mmol) was added andstirring was continued at RT overnight, TLC (DCM:MeOH=10:1) showed thatsome of the 28a remained. NaCNBH₃ (1.2 equiv) was added and the mixturewas heated at 40° C. overnight, TLC (DCM:MeOH=10:1) showed that most ofthe ketone was consumed. The mixture was washed twice with brine, driedover Na₂SO₄, filtered and concentrated in vacuo. The residue waspurified by silica column (DCM: MeOH=100:1 to 50:1) to give 84a (90 mg,18%) as a yellow solid. LC-MS (Agilent): R_(t) 3.28 min; m/z calculatedfor C₃₄H₃₉N₃O₃ [M+H]⁺ 538.4, found [M+H]⁺ 538.4.

7. Procedure for the Preparation of 84

To a mixture of 84a (90 mg, 0.17 mmol) in THF/water (6 mL/2 mL) wasadded LiOH.H₂O (21 mg, 0.51 mmol) and the mixture was stirred at RTovernight, TLC (DCM:MeOH=20:1) showed the starting material wasconsumed. Most of the THF was removed in vacuo, the residue wasdissolved in water (15 mL) and washed with Et₂O (10 mL×2). The aqueouslayer was then acidified to pH=2-3 with a 1 M aqueous HCl solution andextracted with DCM (10 mL×3). The combined organic extracts were washedwith brine, dried over Na₂SO₄, filtered and concentrated in vacuo andthe residue was purified by prep-HPLC to give 84 (25 mg, 28%) as a whitesolid. LC-MS (Agilent): R_(t) 3.29 min; in/z calculated for C₃₃H₃₇N₃O₃[M+H]⁺ 524.28, found [M+H]⁺ 524.3. HPLC (JULY-L) (214 and 254 nm): R_(t)8.67 min.

Example 83: Compound 85(2S,4S)-4-((4aR,7aR)-6-benzoctahydro-1H-pyrrolo[3,4-b]-pyridin-1-yl)-1-(2,2-diphenylacetyl)pyrrolidine-2-carboxylicacid

2. Procedure for the Preparation of 85a

To a solution of 28a (417 mg, 1.24 mmol), amine (300 mg, 1.00 mmol) andEt₃N (230 mg, 2.28 mmol) in MeOH (15 mL) was added AcOH (1.0 mL) and themixture was stirred at RT for 1 h. NaCNBH₃ (80 mg, 1.24 mmol) was thenadded and the mixture was stirred at RT overnight, TLC (DCM:MeOH=10:1)showed that the starting material was consumed. Most of the MeOH wasremoved in vacuo and the residue was dissolved in water (10 mL) andextracted with DCM (10 mL). The organic layer was washed with brine (10mL), dried over Na₂SO₄, filtered and concentrated in vacuo. The residuewas purified by silica column (DCM:MeOH=80:1) to give 85a (220 mg, 33%)as a white solid. LC-MS (Agilent): R_(t) 3.30 min; m/z calculated forC₃₄H₃₉N₃O₃ [M+H]⁺ 538.3, found [M+H]⁺ 538.3.

3. Procedure for the Preparation of 85

To a mixture of 85a (220 mg, 0.41 mmol) in THF/water (10 mL/1.5 mL) wasadded LiOH.H₂O (52 mg, 1.23 mmol) and the mixture was stirred at RTovernight, TLC (DCM:MeOH=10:1) showed that the starting material wasconsumed. Most of the THF was removed in vacuo and the residue wasdissolved in water (15 mL) and acidified to pH=3˜4 with a 3 M aqueousHCl solution. The resulting precipitate was collected by filtration thenpurified by prep-HPLC to give 85 (66 mg, 30%) as a white solid. LC-MS(Agilent): R_(t) 3.28 min; in/z calculated for C₃₃H₃₇N₃O₃ [M+H]⁺ 524.3,found [M+H]⁺ 524.3. HPLC (JULY-L) (214 and 254 nm): R_(t) 8.75 min.

Example 84: Compound 86(3S,3′S,5′S)-1-(2,2-diphenylacetyl)-3-(phenyl-[1,3′-bipyrrolidine]-5′-carboxylicacid

1. Procedure for the Preparation of 86a

To a stirred mixture of (S)-3-phenyl-pyrolidine.hydrochloride (528 mg,2.8 mmol) in CH₃CN (10 mL) was added Et₃N (285 mg, 2.8 mmol) followed by2c (600 mg, 1.4 mmol) and the mixture was heated at 110° C. in a sealedtube overnight. The solvent was removed in vacuo and the residue waspartitioned between water (20 mL) and EA (15 mL). The aqueous layer wasseparated and further extracted with EA (15 mL). The combined organicextracts were washed with brine, dried over Na₂SO₄, filtered andconcentrated in vacuo. The residue was purified by silica column(DCM:MeOH=100:1 to 50:1) to give 86a (230 mg, 35%) as a yellow solid.LC-MS (Agilent): R_(t) 3.27 min; m/z calculated for C₃₀H₃₂N₂O₃ [M+H]⁺469.24, found [M+H]⁺ 469.3.

2. Procedure for the Preparation of 86

To a mixture of 86a (220 mg, 0.47 mmol) in THF/water (8 mL/3 mL) wasadded LiOH.H₂O (59 mg, 1.41 mmol) and the mixture was stirred at RTovernight, TLC (DCM:MeOH=20:1) showed the starting material wasconsumed. Most of the THF was removed in vacuo and the residue wasdissolved in water (20 mL) and washed with Et₂O (15 mL×2). The aqueouslayer was then acidified to pH=2-3 with a 1 M aqueous HCl solution andextracted with DCM (15 mL×2). The combined organic extracts were washedwith brine, dried over Na₂SO₄, filtered and concentrated in vacuo. Theresidue was purified by prep-HPLC to give 86 (50 mg, 23%) as a whitesolid. LC-MS (Agilent): R_(t) 3.53 min; m/z calculated for C₂₉H₃₀N₂O₃[M+H]⁺ 455.24, found [M+H]⁺ 455.3. HPLC (JULY-L) (214 and 254 nm): R_(t)8.80 min.

Example 85: Compound 87(3R,3′S,5′S)-1-(2,2-diphenylacetyl)-3-(phenyl-[1,3′-bipyrrolidine]-5′-carboxylicacid

1. Procedure for the Preparation of 87a

A mixture of 2c (500 mg, 1.19 mmol), (R)-3-phenylpyrrolidinehydrochloride (660 mg 3.59 mmol) and Et₃N (363 mg, 3.59 mmol) in CH₃CN(10 mL) was heated at 110° C. in a sealed tube overnight, TLC(DCM:MeOH=10:1) showed most of the starting material was consumed. Themixture was cooled to RT, concentrated in vacuo and the residue waspurified by chromatography (DCM:MeOH=1:0 to 50:1) to give 87a (200 mg,35%) as a white solid. LC-MS (Agilent): R_(t) 3.35 min; m/z calculatedfor C₃₀H₃₂N₂O₃ [M+H]⁺ 469.2, found [M+H]⁺ 469.3.

2. Procedure for the Preparation of 87

To a mixture of 87a (200 mg, 0.43 mmol) in THF/water (5 mL/1 mL) wasadded LiOH.H₂O (54 mg, 1.28 mmol) and the mixture was stirred at RTovernight, TLC (DCM:MeOH=10:1) showed the starting material wasconsumed. Most of the THF was removed in vacuo and the residue wasdissolved in water (15 mL) and washed with ether (15 mL×2). The aqueouslayer was then cooled in an ice water bath and acidified to pH=3′4 witha 1 M aqueous HCl solution. The resulting precipitate was collected byfiltration, washed with water (5 mL×3) and dried at 45° C. overnight togive 87 (70 mg, 36%) as a white solid. LC-MS (Agilent): R_(t) 3.48 min;m/z calculated for C₂₉H₃₀N₂O₃ [M+H]⁺ 455.2, found [M+H]⁺ 455.3. HPLC(JULY-L) (214 and 254 nm): R_(t) 8.77 min.

Biological Example 1: AT₂ Receptor Binding

Media and Solutions

-   -   1. Trypsin-EDTA (for preparation of 100 mL)        -   Trypsin 0.25 g        -   2% EDTA 2 mL        -   PBS 98 mL        -   Dissolve trypsin in 2% EDTA and PBS completely; sterilize            the solution by passing through a 0.20 μM membrane filter;            store at 4° C.    -   2. DMEM medium (for preparation of 1 L)        -   The powder was dissolved into 950 mL of distilled water with            gentle stirring until the solution becomes clear.        -   Add. NaHCO₃ 1.176 g for DMEM medium.        -   Adjust pH of medium to 0.2-0.3 below final working pH using            1 M NaOH or 1 M        -   HCl. Add slowly with stirring.        -   Dilute to 1 liter with ddH₂O.        -   Sterilize the medium immediately by filtration.        -   Store at 4° C.    -   3. TE buffer        -   20 mM Tris-HCl, pH 7.4,        -   5 mM EDTA    -   4. Binding Assay Buffer        -   50 mM Hepes, pH 7.4        -   5 mM MgCl₂        -   1 mM CaCl₂        -   0.2% BSA    -   5. Wash Buffer        -   50 mM Hepes, pH 7.4

Procedures for HEK293/AT₂ Receptor Transient Cell

Transfection

-   -   Cells were plated into 150 mm dish at 50% density for transient        transfection. Cells were ready for transfection after overnight        incubation (the confluence reaches around 80%).    -   75 μL Lipofectamine™2000 diluted in 6.25 mL OptiMEM I Reduced        Serum Medium, was mixed gently, and incubated at room        temperature for 5 minutes. 50 μg expression plasmid DNA diluted        in 6.25 mL OptiMEM I Reduced Serum Medium without serum was        mixed gently.    -   After the 5 minute incubation, the diluted DNA was combined with        the diluted Lipofectamine™2000 (total volume is 12.5 mL). The        mixture was mixed gently and incubated for 30 minutes at room        temperature to allow the DNA-Lipofectamine™2000 complexes to        form.    -   The 12.5 mL DNA-Lipofectamine™ 2000 complexes were added into        the 150 mm dish and mixed gently by rocking the dish back and        forth.    -   The cells were incubated at 37° C. with 5% CO₂ for 48 hours.    -   Cells were collected and stored frozen at −80° C.

Procedures for HEK293/AT₂ Receptor Cell Membrane Preparation

-   -   Frozen HEK293/AT₂ receptor (transient transfected) cells were        homogenized in ice cold TE buffer for 10 s.    -   The homogenate was centrifuged at 25,000 g for 30 minutes.    -   The pellet was resuspended in ice cold tissue buffer.    -   Protein concentrations were determined using Bradford assay        method with BSA as standard.    -   The membrane protein was frozen under −80° C.

Compound Preparation

Solutions of all compounds were prepared bymicroplate liquid handlingequipment such as Janus or Precision 2000. Compounds, dissolved in DMSOwere stored in a Freezer. Compounds were prepared from 30 mM in 100%DMSO.

Step 1: Dose Plate Preparation (96 Well Plate)

-   -   Add the 3 μL [30 mM] compound stock to column 1 on the plate.    -   Add 15 pt of 100% DMSO to column 1.    -   Add 10.81 μL of 100% DMSO to column 2-12.    -   Transfer 5 μL from column 1 into column 2 (half log dilution).    -   Transfer 5 μL from column 2 into column 3 (half log dilution).    -   Transfer 5 μL from column 3 into column 4 (half log dilution).    -   Transfer 5 μL from column 4 into column 5 (half log dilution).    -   Transfer 5 μL from column 5 into column 6 (half log dilution).    -   Transfer 5 μL from column 6 into column 7 (half log dilution).    -   Transfer 5 μL from column 7 into column 8 (half log dilution).    -   Transfer 5 μL from column 8 into column 9 (half log dilution).    -   Transfer 5 μL from column 9 into column 10 (half log dilution)    -   Transfer 5 μL from column 10 into column 11 (half log dilution)    -   Transfer 5 μL from column 11 into column 12 (half log dilution).

All the compounds were diluted using Precision 2000 microplate liquidhandling equipment. The top concentration of compound was 5 mM with 100%DMSO.

Step 2: Working Plate Preparation (96 Well Plate)

-   -   Compounds were diluted 50-fold with buffer.    -   49 μL buffer was added to the well of 96 well plate.    -   1 μL compound solution from dose plate was transferred to the        corresponding well of working plate.    -   The top concentration of compound was 100 μM with 2% DMSO.

Step 3: Assay Plate Preparation (96 Well Plate)

15 μL of compound solution was transferred from each well of workingplate to the well of assay plate by Janus. Each compound was assayed induplicate in each plate and there were 4 compounds per plate.

Procedures for AT₂ Receptor Binding Assay

-   -   120 μL membrane (5 mg protein/well) was incubated with 15 μL of        [¹²⁵I] CGP42112A and 15 μL of compound at RT for 1.5 hrs.    -   The binding reaction was stopped by rapid filtration through        Unifilter GF/C plates (presoaked in 0.3% (v:v) BSA).    -   Plate was washed three times with ice cold wash buffer.    -   The filtration plates were dried at 37° C. overnight.    -   50 μL of scintillation cocktail was added to each well.    -   Radioactivity was determined using MicroBetaTriluxmicroplate        scintillation counter.

Data Analysis

Data was analyzed through 4 parameter logic using Prism 5.0 software.

The results are shown in the following Table:

Compound IC₅₀ (nM)  2 113.9  3 192.9  5 89.96  6 181.3  9 98.62  1554.47  16 6654  17 3974  21 62.14  22 384.1  23 290.3  28 86.86  35539.9  36 1664  46 2257  48 89.43  49 58.81  50 67.27  51 50.33  5343.88  54 154.8  55 386.4  56 315.5  58 3050  61-A 83.34  61-B 107.0  62540.2  63 482.9  64 3358  65 1605  67 3665  70-B 1340  70-A 49.08  753829  76 3604  84 75.75  85 102.6  86 817.4  87 43.6  90 64.23  91 12.01 92 133.8  93 125.6  8 512.1  96 2248  97 457.5  98 240.5  99 535.5 10018 101 400.5 102 498.6 104 1316 105 2489 106 426.2 107 461 108 2054 109650.4 112 255.1 114 17.05  52 63.23 115 321.3 116 649.6 118 313.7 1192647 120 1199 121 57.67 122 142.6 124 363.4 125 1244 126 20.48 131 652.1133 1738 134 954.5 135 240.2 136 89.03 137 173.4 138 3.519 139 2533 140673.7 142 992.9 143 372.3

Biological Example 2: AT₁ Receptor Binding

The same media, solutions, cell procedures and compound preparation wasused as for Biological Example 1 but using HEK293/AT₁ Receptor TransientCells. The binding assay was then performed as follows:

-   -   120 μL membrane (5 mg protein/well) was incubated with 15 μL of        [¹²⁵I]-Sar1-Ile8-Angiotensin II and 15 μL of compound at RT for        1.5 hrs.    -   The binding reaction was stopped by rapid filtration through        Unifilter GF/C plates (presoaked in 0.3% (v:v) BSA).    -   Plate was washed three times with ice cold wash buffer.    -   The filtration plates were dried at 37° C. overnight.    -   50 μL of scintillation cocktail was added to each well.    -   Radioactivity was determined using MicroBetaTriluxmicroplate        scintillation counter.

The IC₅₀ binding results for a known selective AT₂ receptor antagonistPD-126,055, known selective AT₁ receptor antagonist, Losartin,angiotensin II and compound 21 are shown in the following Table.

Compound IC₅₀ (nM) Ki (nM) PD-126,055 — — Compound 21 — — Losartin 11.015.505 Angiotensin II 1.797 0.8985 —: No significant inhibition ofbinding of the radiolabelled ligand even at top concentration tested (10μM). Compounds 6, 112, 136 and 138 were also analysed in a similar assayand showed no AT₁ receptor binding at 10 μM.

Biological Example 3: AT₂ Receptor Neurite Outgrowth Assay

The general methodology of Wallinder (2008) and references cited thereinwas used to assess the effect of the compounds of the present inventionon neurite outgrowth. The assay was adapted for high content screening.

The compounds screened against NG108-15 neurite cells were the known AT₂selective antagonist PD-126,055, compound 6, compound 15, compound 21and compound 28. The controls used were naïve cells, DMSO 0.2% treatedcells, cells treated with Angiotensin II (Ang II) 0.1 μM, EMA1087 0.1 μMand Ang II 0.1 μM+PD-123,319 (PD-123) 1 μM. EMA1087 is a known AT₂receptor agonist described as “compound 21” in Wan et al. 2004.PD-123,319 is a known, commercially available AT₂ receptor antagonist.The results were analyzed by immunofluorescence quantitative analysis.Neurite outgrowth was quantified with neurite average length usingCellomics software. Results are expressed as the mean±SEM, eachconducted in triplicate. Statistical significance, compared with Ang IIcontrol: *p<0.05, **p<0.01, and ***p<0.001. NS: no significantdifference. ND: not determined. FIGS. 1 to 5 show neurite outgrowth wasinhibited by the AT₂ receptor antagonists, PD-126,055 and compounds 6,15, 21 and 28.

REFERENCES

-   Chakrabarty et al., 2008, Estrogen elicits dorsal root ganglion axon    sprouting via a rennin-angiotensin system. Endocrinology,    149(7):3452-3460.-   Clere et al., 2010, Deficiency or blockade of angiotensin II type 2    receptor delays tumorigenesis by inhibiting malignant cell    proliferation and angiogenesis. Int. J. Cancer, 127: 2279-2291.-   Izu et al., 2009, Angiotensin II Type 2 receptor blockade increases    bone mass. J. Biol. Chem., 284(8):4857-4864.-   Steckelings et al., 2005, The AT₂ receptor A matter of love and    hate. Peptides, 26:1401-1409.-   Wallinder et al., 2008, Selective angiotensin II AT₂ receptor    agonists: Benzamide structure-activity relationships. Bioorganic &    Medicinal Chemistry, 16:6841-6849.-   Wan et al., 2004, Design, Synthesis and biological evaluation of the    first selective nonpeptide AT₂ receptor agonist. J. Med. Chem.,    47:5995-6008.-   Wexler et al., 1996, Nonpeptide angiotensin II receptor antagonists:    The next generation in antihypertensive therapy. J. Med. Chem.,    39(3):325-656.

1. A compound of formula (I):

wherein: X is absent and Y is —CHR³CH₂—, —CH₂CHR³—, —CHR³CHR⁴CH₂—,—CH₂CHR³CHR⁴—, —CH₂CH₂CHR³—, —CR³═CHCH₂—, —CH═CHR³CH₂— or —CH₂CH═CR³—;or X is —CHR⁵ and Y is —CHR³—, —CHR³CHR⁴—, —CHR³CR⁴═, —CH₂CHR³—,—CR³═CH— or —CH═CR³—, wherein when Y is —CHR³CR⁴═, R^(2b) is absent, orX is —CH₂CHR⁵— or C(═O)CHR⁵— and Y is —CHR³—; R¹ is —C(═O)CHR⁶R⁷,—C(═O)NR⁶R⁷, —C(═O)CH₂CHR⁶R⁷, —C(═O)CH═CR⁶R⁷, —C(═S)CHR⁶R⁷, —C(═S)NR⁶R⁷,—C(═S)CH₂CHR⁶R⁷, —C(═S)CH═CR⁶R⁷, —C(═NR⁸)CHR⁶R⁷, —C(═NR⁸)NR⁶R⁷,—C(═NR⁸)CH₂CHR⁶R⁷ or —C(═NR⁸)CH—CR⁶R⁷; R² is —C₁₋₆alkyl, —C₂₋₆alkenyl,—C₂₋₆alkynyl, —OR⁸, —SR⁸, —N(R⁸)₂, —C(═O)R⁸, —C(═O)N(R⁸)₂,—N(R⁸)C(═O)R⁸, —N(R⁸)C(═O)N(R⁸)₂, —N(R⁸)SO₂R⁸, —SO₂N(R⁸)₂,—N(R⁸)SO₂N(R⁸)₂, —W-cycloalkyl, —W-cycloalkenyl, —W-aryl,—W-heterocyclyl, —W-heteroaryl, —W—Z—W-cycloalkyl, —W—Z—W-cycloalkenyl,—W—Z—W-aryl, —W—Z—W-heterocyclyl or —W—Z—W-heteroaryl, ═CH—C(═O)-J-R¹⁰,═CHC(═O)NH-J-R¹⁰, —OCH₂CHR¹⁰CH₂R¹⁰ or —OCH₂C(R¹⁰)═CHR¹⁰; R^(2b) ishydrogen; R³ is a carboxylic acid, —CH₂CO₂H, —C(═O)C(═O)OH, —CH₂OH,—C(═O)NH₂, —CN, —CH₂C(═O)NH₂, —CH₂CN, a carboxylic acid bioisostere or—CH₂carboxylic acid bioisostere; R⁴ is hydrogen or R³ and R⁴ togetherform a group:

where R¹¹ is a carboxylic acid, —CH₂CO₂H, —C(═O)C(═O)OH, —CH₂OH,—C(═O)NH₂, —CN, —CH₂C(═O)NH₂, —CH₂CN, a carboxylic acid bioisostere or—CH₂carboxylic acid bioisostere; R⁵ is hydrogen or together with R²forms a fused aryl, heterocyclyl or heteroaryl ring, optionallysubstituted with one or two optional substituents selected from—C₁₋₆alkyl, —C₂₋₆alkenyl, —C₂₋₆alkynyl, cycloalkyl, cycloalkenyl, aryl,heterocyclyl, heteroaryl, —C₁₋₆alkyleneR¹⁰, —C₂₋₆alkenyleneR¹⁰,—C₂₋₆alkynyleneR¹⁰, —OCF₃, —OCHF₂, —OR⁹, —OC₁₋₆alkyleneR¹⁰,—OC₂₋₆alkenyleneR¹⁰, —OC₂₋₆alkynyleneR¹⁰, —SO₂NHR⁹, —NHSO₂R⁹,—NHC(═O)NHR⁹, —NHC(═O)OR⁹ or —CH(OH)CH(OH)R⁹; R⁶ and R⁷ areindependently hydrogen, —C₁₋₆alkyl, cycloalkyl, cycloalkenyl, aryl,heterocyclyl, heteroaryl, —CH₂aryl, —CH₂cycloalkyl, —CH₂cycloalkenyl,—CH₂heterocyclyl or —CH₂heteroaryl; provided that R⁶ and R⁷ are not bothhydrogen; R⁸ is hydrogen, —C₁₋₈alkyl, —C₁₋₈fluoroalkyl, aryl,—C₁₋₈alkylenearyl, —C₂₋₈alkenylenearyl or —C₂₋₈alkyylenearyl; R⁹ is—C₁₋₆alkyl, —C₂₋₆alkenyl, —C₂₋₆alkynyl, cycloalkyl, cycloalkenyl, aryl,heterocyclyl, heteroaryl, arylcycloalkyl-, arylcycloalkenyl-, arylaryl-,arylheterocyclyl- or arylheteroaryl-; W is a covalent bond, —O—, —S—,—SO—, —SO₂—N(R⁸)—, —C(═O)—, —N(R⁸)C(═O)—, —C(═O)N(R⁸)—, —C₁₋₄alkylene-,—C₂₋₄alkenylene-, —C₂₋₄alkynylene-, —C₁₋₃alkyleneQC₁₋₃alkylene-,-QC₁₋₄alkylene-, -QC₂₋₄alkenylene-, -QC₂₋₄alkynylene-, —C₁₋₄alkyleneQ-,—C₂₋₄alkenyleneQ-, —C₂₋₄alkynyleneQ-QC₁₋₄alkyleneQ-, -QC₂₋₄alkenyleneQ-or —OC₂₋₄alkynyleneQ-; Q is —O—, —S—, —SO—, —SO₂—N(R⁸)—, —C(═O)—,—N(R⁸)C(═O)—, —C(═O)N(R⁸)—, Z is -cycloalkyl-, -cycloalkenyl-, -aryl-,-heterocyclyl- or -heteroaryl-; J is a covalent bond or —C₁₋₆alkylene-,—C₂₋₆alkenylene- or —C₂₋₆alkynylene, in which one —CH₂— group in thealkylene, alkenylene or alkynylene group may be replaced by —O—, —S—,—S(O)—, —S(O)₂—N(R⁸)—, —C(═O)—, —C(═O)NH— or —NHC(═O)—; R¹⁹ iscycloalkyl, cycloalkenyl, aryl, heterocyclyl or heteroaryl; and whereineach cycloalkyl, cycloalkenyl, aryl, heterocyclyl and heteroaryl may beoptionally substituted; or a pharmaceutically acceptable salt thereof.2. A compound according to claim 1 wherein X is absent and Y is—CHR³CH²— or X is —CH₂— and Y is —CHR³—.
 3. A compound according toclaim 1 wherein X is absent and Y is —CHR³CHR⁴CH₂—, —CH₂CHR³CHR⁴— or—CH₂CH₂CHR³— or X is —CHR⁵— and Y is —CHR³CHR⁴—, —CH₂CHR³—, —CHR³═CH— or—CH═CHR³— or X is —CH₂CHR⁵— and Y is —CHR³—.
 4. A compound according toclaim 1 wherein R¹ is —C(═O)CH(aryl)(aryl), —C(═O)CH(aryl)(cycloalkyl),—C(═O)CH(cycloalkyl)(cycloalkyl), —C(═O)N(aryl)(aryl),—C(═O)N(aryl)(cycloalkyl) or —C(═O)N(cycloalkyl)(cycloalkyl).
 5. Acompound according to claim 4 wherein R¹ is —C(═O)CH(phenyl)(phenyl),—C(═O)CH(phenyl)(cyclohexyl), —C(═O)CH(cyclohexyl)(cyclohexyl),—C(═O)N(phenyl)(phenyl), —C(═O)N(phenyl)(cyclohexyl) or—C(═O)N(cyclohexyl)(cyclohexyl) wherein each phenyl or cyclohexyl isoptionally substituted with one or more substituents selected from—C₁₋₃alkyl, —OC₁₋₃alkyl and halo.
 6. A compound according to claim 1wherein R² is cycloalkyl, cycloalkenyl, aryl, heterocyclyl, heteroaryl,-heterocyclylaryl, -heterocyclylC₁₋₃alkylenearyl,—C₁₋₄alkylenecycloalkyl, —C₁₋₄alkylenecycloalkenyl, —C₁₋₄alkylenearyl,—C₁₋₄alkyleneheterocyclyl, —C₁₋₄alkyleneheteroaryl,—C₂₋₄alkenylenecycloalkyl, —C₂₋₄alkenylenecycloalkenyl,—C₂₋₄alkenylenearyl, —C₂₋₄alkenyleneheterocyclyl,—C₂₋₄alkenyleneheteroaryl, —C₂₋₄alkynylenecycloalkyl,—C₂₋₄alkynylenecycloalkenyl, —C₂₋₄alkynylenearyl,—C₂₋₄alkynyleneheterocyclyl, —C₂₋₄alkynyleneheteroaryl,═CHC(═O)NHCH₂cycloalkyl, ═CHC(═O)NHCH₂cycloalkenyl, ═CHC(═O)NHCH₂aryl,═CHC(═O)NHCH₂heterocyclyl, ═CHC(═O)NHCH₂heteroaryl, —Ocycloalkyl,—Ocycloalkenyl, —Oaryl, —Oheterocyclyl, —Oheteroaryl,—OC₁₋₃alkylenecycloalkyl, —OC₁₋₃alkylenecycloalkenyl,—OC₁₋₃alkylenearyl, —OC₁₋₃alkyleneheterocyclyl,—OC₁₋₃alkyleneheteroaryl, —OC₂₋₃alkenylenecycloalkyl,—OC₂₋₃alkenylenecycloalkenyl, —OC₂₋₃alkenylenearyl,—OC₂₋₃alkenyleneheterocyclyl, —OC₂₋₃alkenyleneheteroaryl,—OC₂₋₃alkynylenecycloalkyl, —OC₂₋₃alkynylenecycloalkenyl,—OC₂₋₃alkynylenearyl, —OC₂₋₃alkynyleneheterocyclyl,—OC₂₋₃alkynyleneheteroaryl, —OC₁₋₃alkylenecycloalkylaryl, —OarylOaryl,—OarylOC₁₋₃alkylenearyl, —Scycloalkyl, —Scycloalkenyl, —Saryl,—Sheterocyclyl, —Sheteroaryl, —SC₁₋₃alkylenecycloalkyl,—SC₁₋₃alkylenecycloalkenyl, —SC₁₋₃alkylenearyl,—SC₁₋₃alkyleneheterocyclyl, —SC₁₋₃alkyleneheteroaryl,—SC₂₋₃alkenylenecycloalkyl, —SC₂₋₃alkenylenecycloalkenyl,—SC₂₋₃alkenylenearyl, —SC₂₋₃alkenyleneheterocyclyl,—SC₂₋₃alkenyleneheteroaryl, —SC₂₋₃alkynylenecycloalkyl,—SC₂₋₃alkynylenecycloalkenyl, —SC₂₋₃alkynylenearyl,—SC₂₋₃alkynyleneheterocyclyl, —SC₂₋₃alkynyleneheteroaryl,—SC₁₋₃alkylenecycloalkylaryl, —SO₂cycloalkyl, —SO₂cycloalkenyl,—SO₂aryl, —SO₂heterocyclyl, —SO₂heteroaryl, —SO₂C₁₋₃alkylenecycloalkyl,—SO₂C₁₋₃alkylenecycloalkenyl, —SO₂C₁₋₃alkylenearyl,—SO₂C₁₋₃alkyleneheterocyclyl, —SO₂C₁₋₃alkyleneheteroaryl,—SO₂C₂₋₃alkenylenecycloalkyl, —SO₂C₂₋₃alkenylenecycloalkenyl,—SO₂C₂₋₃alkenylenearyl, —SO₂C₂₋₃alkenyleneheterocyclyl,—SO₂C₂₋₃alkenyleneheteroaryl, —SO₂C₂₋₃alkynylenecycloalkyl,—SO₂C₂₋₃alkynylenecycloalkenyl, —SO₂C₂₋₃alkynylenearyl,—SO₂C₂₋₃alkynyleneheterocyclyl, —SO₂C₂₋₃alkynyleneheteroaryl,—SO₂C₁₋₃alkylenecycloalkylaryl, —NHC₁₋₈alkyl, —NHC₂₋₈alkenyl,—NHC₂₋₈alkynyl, —NHcycloalkyl, —NHcycloalkenyl, —NHaryl,—NHheterocyclyl, —NHheteroaryl, —NHC₁₋₃alkylenecycloalkyl,—NHC₁₋₃alkylenecycloalkenyl, —NHC₁₋₃alkylenearyl,—NHC₁₋₃alkyleneheterocyclyl, —NHC₁₋₃alkyleneheteroaryl,—NHC₂₋₃alkenylenecycloalkyl, —NHC₂₋₃alkenylenecycloalkenyl,—NHC₂₋₃alkenylenearyl, —NHC₂₋₃alkenyleneheterocyclyl,—NHC₂₋₃alkenyleneheteroaryl, —NHC₂₋₃alkynylenecycloalkyl,—NHC₂₋₃alkynylenecycloalkenyl, —NHC₂₋₃alkynylenearyl,—NHC₂₋₃alkynyleneheterocyclyl, —NHC₂₋₃alkynyleneheteroaryl,—NHC(═O)cycloalkyl, —NHC(═O)cycloalkenyl, —NHC(═O)aryl,—NHC(═O)heterocyclyl, —NHC(═O)heteroaryl,—NHC(═O)C₁₋₃alkylenecycloalkyl, —NHC(═O)C₁₋₃alkylenecycloalkenyl,—NHC(═O)C₁₋₃alkylenearyl, —NHC(═O)C₁₋₃alkyleneheterocyclyl,—NHC(═O)C₁₋₃alkyleneheteroaryl, —NHC(═O)C₂₋₃alkenylenecycloalkyl,—NHC(═O)C₂₋₃alkenylenecycloalkenyl, —NHC(═O)C₂₋₃alkenylenearyl,—NHC(═O)C₂₋₃alkenyleneheterocyclyl, —NHC(═O)C₂₋₃alkenyleneheteroaryl,—NHC(═O)C₂₋₃alkynylenecycloalkyl, —NHC(═O)C₂₋₃alkynylenecycloalkenyl,—NHC(═O)C₂₋₃alkynylenearyl, —NHC(═O)C₂₋₃alkynyleneheterocyclyl,—NHC(═O)C₂₋₃alkynyleneheteroaryl, —N(CH₃)C₁₋₈alkyl, —N(CH₃)C₂₋₈alkenyl,—N(CH₃)C₂₋₈alkynyl, —N(CH₃)cycloalkyl, —N(CH₃)cycloalkenyl, —N(CH₃)aryl,—N(CH₃)heterocyclyl, —N(CH₃)heteroaryl, —N(CH₃)C₁₋₃alkylenecycloalkyl,—N(CH₃)C₁₋₃alkylenecycloalkenyl, —N(CH₃)C₁₋₃alkylenearyl,—N(CH₃)C₁₋₃alkyleneheterocyclyl, —N(CH₃)C₁₋₃alkyleneheteroaryl,—N(CH₃)C₂₋₃alkenylenecycloalkyl, —N(CH₃)C₂₋₃alkenylenecycloalkenyl,—N(CH₃)C₂₋₃alkenylenearyl, —N(CH₃)C₂₋₃alkenyleneheterocyclyl,—N(CH₃)C₂₋₃alkenyleneheteroaryl, —N(CH₃)C₂₋₃alkynylenecycloalkyl,—N(CH₃)C₂₋₃alkynylenecycloalkenyl, —N(CH₃)C₂₋₃alkynylenearyl,—N(CH₃)C₂₋₃alkynyleneheterocyclyl, —N(CH₃)C₂₋₃alkynyleneheteroaryl,—N(CH₃)C(═O)cycloalkyl, —N(CH₃)C(═O)cycloalkenyl, —N(CH₃)C(═O)aryl,—N(CH₃)C(═O)heterocyclyl, —N(CH₃)C(═O)heteroaryl,—N(CH₃)C(═O)C₁₋₃alkylenecycloalkyl,—N(CH₃)C(═O)C₁₋₃alkylenecycloalkenyl, —N(CH₃)C(═O)C₁₋₃alkylenearyl,—N(CH₃)C(═O)C₁₋₃alkyleneheterocyclyl,—N(CH₃)C(═O)C₁₋₃alkyleneheteroaryl,—N(CH₃)C(═O)C₂₋₃alkenylenecycloalkyl,—N(CH₃)C(═O)C₂₋₃alkenylenecycloalkenyl, —N(CH₃)C(═O)C₂₋₃alkenylenearyl,—N(CH₃)C(═O)C₂₋₃alkenyleneheterocyclyl,—N(CH₃)C(═O)C₂₋₃alkenyleneheteroaryl,—N(CH₃)C(═O)C₂₋₃alkynylenecycloalkyl,—N(CH₃)C(═O)C₂₋₃alkynylenecycloalkenyl, —N(CH₃)C(═O)C₂₋₃alkynylenearyl,—N(CH₃)C(═O)C₂₋₃alkynyleneheterocyclyl,—N(CH₃)C(═O)C₂₋₃alkynyleneheteroaryl, —N(C(═O)CH₃)cycloalkyl,—N(C(═O)CH₃)cycloalkenyl, —N(C(═O)CH₃)aryl, —N(C(═O)CH₃)heterocyclyl,—N(C(═O)CH₃)heteroaryl, —N(C(═O)CH₃)C₁₋₃alkylenecycloalkyl,—N(C(═O)CH₃)C₁₋₃alkylenecycloalkenyl, —N(C(═O)CH₃)C₁₋₃alkylenearyl,—N(C(═O)CH₃)C₁₋₃alkyleneheterocyclyl,—N(C(═O)CH₃)C₁₋₃alkyleneheteroaryl,—N(C(═O)CH₃)C₂₋₃alkenylenecycloalkyl,—N(C(═O)CH₃)C₂₋₃alkenylenecycloalkenyl, —N(C(═O)CH₃)C₂₋₃alkenylenearyl,—N(C(═O)CH₃)C₂₋₃alkenyleneheterocyclyl,—N(C(═O)CH₃)C₂₋₃alkenyleneheteroaryl,—N(C(═O)CH₃)C₂₋₃alkynylenecycloalkyl,—N(C(═O)CH₃)C₂₋₃alkynylenecycloalkenyl, —N(C(═O)CH₃)C₂₋₃alkynylenearyl,—N(C(O)CH₃)C₂₋₃alkynyleneheterocyclyl,—N(C(O)CH₃)C₂₋₃alkynyleneheteroaryl, —N(SO₂CH₃)cycloalkyl,—N(SO₂CH₃)cycloalkenyl, —N(SO₂CH₃)aryl, —N(SO₂CH₃)heterocyclyl,—N(SO₂CH₃)heteroaryl, —N(SO₂CH₃)C₁₋₃alkylenecycloalkyl,—N(SO₂CH₃)C₁₋₃alkylenecycloalkenyl, —N(SO₂CH₃)C₁₋₃alkylenearyl,—N(SO₂CH₃)C₁₋₃alkyleneheterocyclyl, —N(SO₂CH₃)C₁₋₃alkyleneheteroaryl,—N(SO₂CH₃)C₂₋₃alkenylenecycloalkyl,—N(SO₂CH₃)C₂₋₃alkenylenecycloalkenyl, —N(SO₂CH₃)C₂₋₃alkenylenearyl,—N(SO₂CH₃)C₂₋₃alkenyleneheterocyclyl,—N(SO₂CH₃)C₂₋₃alkenyleneheteroaryl, —N(SO₂CH₃)C₂₋₃alkynylenecycloalkyl,—N(SO₂CH₃)C₂₋₃alkynylenecycloalkenyl, —N(SO₂CH₃)C₂₋₃alkynylenearyl,—N(SO₂CH₃)C₂₋₃alkynyleneheterocyclyl,—N(SO₂CH₃)C₂₋₃alkynyleneheteroaryl, —N(CH₂CF₃)cycloalkyl,—N(CH₂CF₃)cycloalkenyl, —N(CH₂CF₃)aryl, —N(CH₂CF₃)heterocyclyl,—N(CH₂CF₃)heteroaryl, —N(CH₂CF₃)C₁₋₃alkylenecycloalkyl,—N(CH₂CF₃)C₁₋₃alkylenecycloalkenyl, —N(CH₂CF₃)C₁₋₃alkylenearyl,—N(CH₂CF₃)C₁₋₃alkyleneheterocyclyl, —N(CH₂CF₃)C₁₋₃alkyleneheteroaryl,—N(CH₂CF₃)C₂₋₃alkenylenecycloalkyl,—N(CH₂CF₃)C₂₋₃alkenylenecycloalkenyl, —N(CH₂CF₃)C₂₋₃alkenylenearyl,—N(CH₂CF₃)C₂₋₃alkenyleneheterocyclyl,—N(CH₂CF₃)C₂₋₃alkenyleneheteroaryl, —N(CH₂CF₃)C₂₋₃alkynylenecycloalkyl,—N(CH₂CF₃)C₂₋₃alkynylenecycloalkenyl, —N(CH₂CF₃)C₂₋₃alkynylenearyl,—N(CH₂CF₃)C₂₋₃alkynyleneheterocyclyl,—N(CH₂CF₃)C₂₋₃alkynyleneheteroaryl, —OCH₂CH(phenyl)CH₂(phenyl),—OCH₂C(phenyl)=CH(phenyl), —CH₂C(═O)NHCH₂cycloalkyl,—CH₂C(═O)NHCH₂cycloalkenyl, —CH₂C(═O)NHCH₂aryl,—CH₂C(═O)NHCH₂heterocyclyl, —CH₂C(═O)NHCH₂heteroaryl,—C(═O)NHC₁₋₃alkylenecycloalkyl, —C(═O)NHC₁₋₃alkylenecycloalkenyl,—C(═O)NHC₁₋₃alkylenearyl, —C(═O)NHC₁₋₃alkyleneheterocyclyl,—C(═O)NHC₁₋₃alkyleneheteroaryl, —CH₂SO₂C₀₋₃alkylenecycloalkyl,—CH₂SO₂C₀₋₃alkylenecycloalkenyl, —CH₂SO₂C₀₋₃alkylenearyl,—CH₂SO₂C₀₋₃alkyleneheterocyclyl, —CH₂SO₂C₀₋₃alkyleneheteroaryl,—CH₂OC₁₋₃alkylenecycloalkyl, —CH₂OC₁₋₃alkylenecycloalkenyl,—CH₂OC₁₋₃alkylenearyl, —CH₂OC₁₋₃alkyleneheterocyclyl,—CH₂OC₁₋₃alkyleneheteroaryl, —CH₂SC₁₋₃alkylenecycloalkyl,—CH₂SC₁₋₃alkylenecycloalkenyl, —CH₂SC₁₋₃alkylenearyl,—CH₂SC₁₋₃alkyleneheterocyclyl, —CH₂SC₁₋₃alkyleneheteroaryl,—CH₂SC₂₋₃alkenylenecycloalkyl, —CH₂SC₂₋₃alkenylenecycloalkenyl,—CH₂SC₂₋₃alkenylenearyl, —CH₂SC₂₋₃alkenyleneheterocyclyl,—CH₂SC₂₋₃alkenyleneheteroaryl, —CH₂SC₂₋₃alkynylenecycloalkyl,—CH₂SC₂₋₃alkynylenecycloalkenyl, —CH₂SC₂₋₃alkynylenearyl,—CH₂SC₂₋₃alkynyleneheterocyclyl, —CH₂SC₂₋₃alkynyleneheteroaryl or—NHC(═O)N(aryl)₂, wherein each cycloalkyl, cycloalkenyl, aryl,heterocyclyl and heteroaryl is optionally substituted.
 7. A compoundaccording to claim 1 wherein R³ is —CO₂H, —CH₂CO₂H, —C(═O)C(═O)OH,—C(═O)NHSO₂C₁₋₆alkyl, —C(═O)NHSO₂phenyl, —C(═O)NHSO₂CF₃—SO₃H or PO₃H₂.8. A compound according to claim 7 wherein R³ is —CO₂H.
 9. A compoundaccording to claim 1 wherein R⁴ is H.
 10. A compound according to claim1 wherein R³ and R⁴ together form:


11. A compound according to claim 1 wherein R⁵ is hydrogen.
 12. Acompound according to claim 1 wherein R² and R⁵ together form an aryl,heteroaryl or heterocyclyl ring selected from:

wherein * indicates the fused bond and R is selected from —C₁₋₃alkyl,—OCF₃, —OCHF₂, —OCH₂phenyl, —CH═CHphenyl, —CH₂CH₂phenyl,—CH(OH)CH(OH)phenyl, —C≡Cphenyl, —SO₂NHphenyl, —NHSO₂phenyl,—NHC(O)NHphenyl, —NHC(O)Ophenyl, —CH₂phenyl, —Ophenyl, —OCH₂CH═CHphenyl,—OCH₂CH₂phenyl, —OCH₂CH₂CH₂phenyl and -phenyl.
 13. A pharmaceuticalcomposition comprising a compound of formula (I) according to claim 1 ora pharmaceutically acceptable salt thereof and a pharmaceuticallyacceptable carrier.
 14. A method of treating or preventing neuropathicpain in a subject comprising administering a compound of formula (I)according to claim 1 or a pharmaceutically acceptable salt thereof. 15.A method of treating or preventing a condition characterized by neuronalhypersensitivity in a subject comprising administering a compound offormula (I) according to claim 1 or a pharmaceutically acceptable saltthereof.
 16. A method of treating or preventing inflammatory pain in asubject comprising administering a compound of formula (I) according toclaim 1 or a pharmaceutically acceptable salt thereof.
 17. A method oftreating or preventing impaired nerve conduction velocity in a subjectcomprising administering a compound of formula (I) according to claim 1or a pharmaceutically acceptable salt thereof.
 18. A method of producinganalgesia in a subject comprising administering a compound of formula(I) according to claim 1 or a pharmaceutically acceptable salt thereof.19. A method of treating or preventing a cell proliferative disorder ina subject comprising administering a compound of formula (I) accordingto claim 1 or a pharmaceutically acceptable salt thereof.
 20. A methodof treating or preventing a disorder associated with an imbalancebetween bone resorption and bone formation in a subject comprisingadministering a compound of formula (I) according to claim 1 or apharmaceutically acceptable salt thereof.
 21. A method of treating adisorder associated with aberrant nerve regeneration in a subjectcomprising administering a compound of formula (I) according to claim 1or a pharmaceutically acceptable salt thereof.